Hobbs Medical Recalls
73 recalls on record · June 13, 2018 to November 27, 2024 · Medical Devices
Recalls by year
18
22
24
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
November 27, 2024Medical DevicesFDA
Hobbs Medical, Inc. recalls Posi-Stop Injection Needle, 25 Gauge, Catalog Number: 4723
Hazard: Injection solutions would not flow as intended through the tip of 25ga-sized needles. Investigations that some units contained debris from the manufacturing process within the inner sheath that blocked the ID of the needle.
November 27, 2024Medical DevicesFDA
Hobbs Medical, Inc. recalls Posi-Stop Injection Needle, 25 Gauge, Catalog Number: 4722
Hazard: Injection solutions would not flow as intended through the tip of 25ga-sized needles. Investigations that some units contained debris from the manufacturing process within the inner sheath that blocked the ID of the needle.
November 27, 2024Medical DevicesFDA
Hobbs Medical, Inc. recalls Posi-Stop Injection Needle, 25 Gauge, Catalog Number: 4718
Hazard: Injection solutions would not flow as intended through the tip of 25ga-sized needles. Investigations that some units contained debris from the manufacturing process within the inner sheath that blocked the ID of the needle.
November 27, 2024Medical DevicesFDA
Hobbs Medical, Inc. recalls Posi-Stop Injection Needle, 25 Gauge, Catalog Number: 4704
Hazard: Injection solutions would not flow as intended through the tip of 25ga-sized needles. Investigations that some units contained debris from the manufacturing process within the inner sheath that blocked the ID of the needle.
November 27, 2024Medical DevicesFDA
Hobbs Medical, Inc. recalls Posi-Stop Injection Needle, 23 Gauge, Catalog Number: 4721
Hazard: Injection solutions would not flow as intended through the tip of 25ga-sized needles. Investigations that some units contained debris from the manufacturing process within the inner sheath that blocked the ID of the needle.
November 27, 2024Medical DevicesFDA
Hobbs Medical, Inc. recalls Posi-Stop Injection Needle, 23 Gauge, Catalog Number: 4716
Hazard: Injection solutions would not flow as intended through the tip of 25ga-sized needles. Investigations that some units contained debris from the manufacturing process within the inner sheath that blocked the ID of the needle.
November 27, 2024Medical DevicesFDA
Hobbs Medical, Inc. recalls Posi-Stop Injection Needle, 23 Gauge, Catalog Number: 4706
Hazard: Injection solutions would not flow as intended through the tip of 25ga-sized needles. Investigations that some units contained debris from the manufacturing process within the inner sheath that blocked the ID of the needle.
November 27, 2024Medical DevicesFDA
Hobbs Medical, Inc. recalls Posi-Stop Injection Needle, 23 Gauge, Catalog Number: 4702
Hazard: Injection solutions would not flow as intended through the tip of 25ga-sized needles. Investigations that some units contained debris from the manufacturing process within the inner sheath that blocked the ID of the needle.
November 27, 2024Medical DevicesFDA
Hobbs Medical, Inc. recalls Posi-Stop Injection Needle, 23 Gauge, Catalog Number: 4720
Hazard: Injection solutions would not flow as intended through the tip of 25ga-sized needles. Investigations that some units contained debris from the manufacturing process within the inner sheath that blocked the ID of the needle.
October 19, 2022Medical DevicesFDA
Hobbs Medical, Inc. recalls Hobbs Medical Polypectomy Snare Catalog Number: 4575-OLY
Hazard: Device label display an incorrect expiration date, extends the shelf life of the product. Affected product distributed in the United States from 3/25/2018 to 9/28/2020, expiration dates between 2022-11-01 and 2025-09-01 (Devices have a lot number ending in R, or are kits containing at least 1 device with a lot number ending in R.)
October 19, 2022Medical DevicesFDA
Hobbs Medical, Inc. recalls Hobbs Medical Polypectomy Snare Catalog Number: 4565-OLY
Hazard: Device label display an incorrect expiration date, extends the shelf life of the product. Affected product distributed in the United States from 3/25/2018 to 9/28/2020, expiration dates between 2022-11-01 and 2025-09-01 (Devices have a lot number ending in R, or are kits containing at least 1 device with a lot number ending in R.)
October 19, 2022Medical DevicesFDA
Hobbs Medical, Inc. recalls Hobbs Medical Polypectomy Snare Catalog Number: 4563-OLY
Hazard: Device label display an incorrect expiration date, extends the shelf life of the product. Affected product distributed in the United States from 3/25/2018 to 9/28/2020, expiration dates between 2022-11-01 and 2025-09-01 (Devices have a lot number ending in R, or are kits containing at least 1 device with a lot number ending in R.)
October 19, 2022Medical DevicesFDA
Hobbs Medical, Inc. recalls Hobbs Medical Polypectomy Snare Catalog Number: 7202
Hazard: Device label display an incorrect expiration date, extends the shelf life of the product. Affected product distributed in the United States from 3/25/2018 to 9/28/2020, expiration dates between 2022-11-01 and 2025-09-01 (Devices have a lot number ending in R, or are kits containing at least 1 device with a lot number ending in R.)
October 19, 2022Medical DevicesFDA
Hobbs Medical, Inc. recalls Freeman Pancreatic Flexi-Stent (contained in kit 6501) Catalog Number: 6541
Hazard: Device label display an incorrect expiration date, extends the shelf life of the product. Affected product distributed in the United States from 3/25/2018 to 9/28/2020, expiration dates between 2022-11-01 and 2025-09-01 (Devices have a lot number ending in R, or are kits containing at least 1 device with a lot number ending in R.)
October 19, 2022Medical DevicesFDA
Hobbs Medical, Inc. recalls Freeman Pancreatic Flexi-Stent Catalog Number: 6584
Hazard: Device label display an incorrect expiration date, extends the shelf life of the product. Affected product distributed in the United States from 3/25/2018 to 9/28/2020, expiration dates between 2022-11-01 and 2025-09-01 (Devices have a lot number ending in R, or are kits containing at least 1 device with a lot number ending in R.)
October 19, 2022Medical DevicesFDA
Hobbs Medical, Inc. recalls Freeman Pancreatic Flexi-Stent Catalog Number: 6582
Hazard: Device label display an incorrect expiration date, extends the shelf life of the product. Affected product distributed in the United States from 3/25/2018 to 9/28/2020, expiration dates between 2022-11-01 and 2025-09-01 (Devices have a lot number ending in R, or are kits containing at least 1 device with a lot number ending in R.)
October 19, 2022Medical DevicesFDA
Hobbs Medical, Inc. recalls Freeman Pancreatic Flexi-Stent Catalog Number: 6568
Hazard: Device label display an incorrect expiration date, extends the shelf life of the product. Affected product distributed in the United States from 3/25/2018 to 9/28/2020, expiration dates between 2022-11-01 and 2025-09-01 (Devices have a lot number ending in R, or are kits containing at least 1 device with a lot number ending in R.)
October 19, 2022Medical DevicesFDA
Hobbs Medical, Inc. recalls Freeman Pancreatic Flexi-Stent Catalog Number: 6567
Hazard: Device label display an incorrect expiration date, extends the shelf life of the product. Affected product distributed in the United States from 3/25/2018 to 9/28/2020, expiration dates between 2022-11-01 and 2025-09-01 (Devices have a lot number ending in R, or are kits containing at least 1 device with a lot number ending in R.)
October 19, 2022Medical DevicesFDA
Hobbs Medical, Inc. recalls Freeman Pancreatic Flexi-Stent Catalog Number: 6566
Hazard: Device label display an incorrect expiration date, extends the shelf life of the product. Affected product distributed in the United States from 3/25/2018 to 9/28/2020, expiration dates between 2022-11-01 and 2025-09-01 (Devices have a lot number ending in R, or are kits containing at least 1 device with a lot number ending in R.)
October 19, 2022Medical DevicesFDA
Hobbs Medical, Inc. recalls Freeman Pancreatic Flexi-Stent Catalog Number: 6562
Hazard: Device label display an incorrect expiration date, extends the shelf life of the product. Affected product distributed in the United States from 3/25/2018 to 9/28/2020, expiration dates between 2022-11-01 and 2025-09-01 (Devices have a lot number ending in R, or are kits containing at least 1 device with a lot number ending in R.)
October 19, 2022Medical DevicesFDA
Hobbs Medical, Inc. recalls Freeman Pancreatic Flexi-Stent Catalog Number: 6548
Hazard: Device label display an incorrect expiration date, extends the shelf life of the product. Affected product distributed in the United States from 3/25/2018 to 9/28/2020, expiration dates between 2022-11-01 and 2025-09-01 (Devices have a lot number ending in R, or are kits containing at least 1 device with a lot number ending in R.)
October 19, 2022Medical DevicesFDA
Hobbs Medical, Inc. recalls Freeman Pancreatic Flexi-Stent Catalog Number: 6544
Hazard: Device label display an incorrect expiration date, extends the shelf life of the product. Affected product distributed in the United States from 3/25/2018 to 9/28/2020, expiration dates between 2022-11-01 and 2025-09-01 (Devices have a lot number ending in R, or are kits containing at least 1 device with a lot number ending in R.)
October 19, 2022Medical DevicesFDA
Hobbs Medical, Inc. recalls Freeman Pancreatic Flexi-Stent Catalog Number: 6535
Hazard: Device label display an incorrect expiration date, extends the shelf life of the product. Affected product distributed in the United States from 3/25/2018 to 9/28/2020, expiration dates between 2022-11-01 and 2025-09-01 (Devices have a lot number ending in R, or are kits containing at least 1 device with a lot number ending in R.)
October 19, 2022Medical DevicesFDA
Hobbs Medical, Inc. recalls Freeman Pancreatic Flexi-Stent Catalog Number: 6534
Hazard: Device label display an incorrect expiration date, extends the shelf life of the product. Affected product distributed in the United States from 3/25/2018 to 9/28/2020, expiration dates between 2022-11-01 and 2025-09-01 (Devices have a lot number ending in R, or are kits containing at least 1 device with a lot number ending in R.)
October 19, 2022Medical DevicesFDA
Hobbs Medical, Inc. recalls Freeman Pancreatic Flexi-Stent Catalog Number: 6533
Hazard: Device label display an incorrect expiration date, extends the shelf life of the product. Affected product distributed in the United States from 3/25/2018 to 9/28/2020, expiration dates between 2022-11-01 and 2025-09-01 (Devices have a lot number ending in R, or are kits containing at least 1 device with a lot number ending in R.)
October 19, 2022Medical DevicesFDA
Hobbs Medical, Inc. recalls Freeman Pancreatic Flexi-Stent Kit (containing 6568) Catalog Number: 6529
Hazard: Device label display an incorrect expiration date, extends the shelf life of the product. Affected product distributed in the United States from 3/25/2018 to 9/28/2020, expiration dates between 2022-11-01 and 2025-09-01 (Devices have a lot number ending in R, or are kits containing at least 1 device with a lot number ending in R.)
October 19, 2022Medical DevicesFDA
Hobbs Medical, Inc. recalls Freeman Pancreatic Flexi-Stent Kit (containing 6567) Catalog Number: 6519
Hazard: Device label display an incorrect expiration date, extends the shelf life of the product. Affected product distributed in the United States from 3/25/2018 to 9/28/2020, expiration dates between 2022-11-01 and 2025-09-01 (Devices have a lot number ending in R, or are kits containing at least 1 device with a lot number ending in R.)
October 19, 2022Medical DevicesFDA
Hobbs Medical, Inc. recalls Freeman Pancreatic Flexi-Stent Kit (containing 6566) Catalog Number: 6518
Hazard: Device label display an incorrect expiration date, extends the shelf life of the product. Affected product distributed in the United States from 3/25/2018 to 9/28/2020, expiration dates between 2022-11-01 and 2025-09-01 (Devices have a lot number ending in R, or are kits containing at least 1 device with a lot number ending in R.)
October 19, 2022Medical DevicesFDA
Hobbs Medical, Inc. recalls Freeman Pancreatic Flexi-Stent Kit (containing 6533) Catalog Number: 6507
Hazard: Device label display an incorrect expiration date, extends the shelf life of the product. Affected product distributed in the United States from 3/25/2018 to 9/28/2020, expiration dates between 2022-11-01 and 2025-09-01 (Devices have a lot number ending in R, or are kits containing at least 1 device with a lot number ending in R.)
October 19, 2022Medical DevicesFDA
Hobbs Medical, Inc. recalls Freeman Pancreatic Flexi-Stent Kits: Single Pigtail (containing 6544) Catalog Number: 6503
Hazard: Device label display an incorrect expiration date, extends the shelf life of the product. Affected product distributed in the United States from 3/25/2018 to 9/28/2020, expiration dates between 2022-11-01 and 2025-09-01 (Devices have a lot number ending in R, or are kits containing at least 1 device with a lot number ending in R.)