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Cardinal Health 200 Recalls
285 recalls on record · October 19, 2016 to August 19, 2026 · Drugs, Medical Devices
Recalls by year
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Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
February 17, 2021Medical DevicesFDA
Cardinal Health 200, LLC recalls Gown Isolation W/Ties Univ Blu, SKU 1200PG, 2200PG, 552200PG Cardinal Health Isolation Gown, Lab Coat, and Kendall" G
Hazard: There is a potential for rips, holes, tears, incomplete and/or open seams, staining, foreign material or debris on the gowns and lab coats.
February 17, 2021Medical DevicesFDA
Cardinal Health 200, LLC recalls Gown Isolation W/Ties Xl Ylw, SKU 1101PG Cardinal Health Isolation Gown, Lab Coat, and Kendall" Gowns are intended to
Hazard: There is a potential for rips, holes, tears, incomplete and/or open seams, staining, foreign material or debris on the gowns and lab coats.
February 17, 2021Medical DevicesFDA
Cardinal Health 200, LLC recalls Gown Isolation W/Ties Univ Ylw, SKU 1100PG, V1100PG, 2100PG, V2100PG, 2150PG, V2100PG Cardinal Health Isolation Gown,
Hazard: There is a potential for rips, holes, tears, incomplete and/or open seams, staining, foreign material or debris on the gowns and lab coats.
February 17, 2021Medical DevicesFDA
Cardinal Health 200, LLC recalls ChemoPlus" Chemo Prep & Admin Kit, CT4025
Hazard: Gowns included in the kits potentially have rips, holes, tears, incomplete and/or open seams, staining, foreign material or debris on the gowns.
February 17, 2021Medical DevicesFDA
Cardinal Health 200, LLC recalls Kendall Spill Kit, 6 Per Case, NonsterileI, BB6016K
Hazard: Gowns included in the kits potentially have rips, holes, tears, incomplete and/or open seams, staining, foreign material or debris on the gowns.
February 17, 2021Medical DevicesFDA
Cardinal Health 200, LLC recalls ChemoPlus Drug Spill Kit-INSTI, SKU DP5016K
Hazard: Gowns included in the kits potentially have rips, holes, tears, incomplete and/or open seams, staining, foreign material or debris on the gowns.
February 17, 2021Medical DevicesFDA
Cardinal Health 200, LLC recalls CHEMOPLUS DRUG SPILL KIT HOS, SKU CT4004
Hazard: Gowns included in the kits potentially have rips, holes, tears, incomplete and/or open seams, staining, foreign material or debris on the gowns.
February 17, 2021Medical DevicesFDA
Cardinal Health 200, LLC recalls CHEMOBLOC Preparation and Administration Kit, Extra Large Blue Gown, Medium and Large Gloves, Nonsterile, SKU DP5106K
Hazard: Gowns included in the kits potentially have rips, holes, tears, incomplete and/or open seams, staining, foreign material or debris on the gowns.
February 17, 2021Medical DevicesFDA
Cardinal Health 200, LLC recalls Covidien ChemoPlus Chemo Spill Kit, Nonsterile, SKU DP5108K
Hazard: Gowns included in the kits potentially have rips, holes, tears, incomplete and/or open seams, staining, foreign material or debris on the gowns.
November 25, 2020Medical DevicesFDA
Cardinal Health 200, LLC recalls Kangaroo Connect 1000ml Bag Set, Non-Sterile, Product Code 77100FD - Product Usage: single-use tubing sets used with pum
Hazard: The feeding spike sets may leak at the interface of the tube and spike connector.
November 25, 2020Medical DevicesFDA
Cardinal Health 200, LLC recalls Kangaroo Connect 500ml Bag Set, Non-Sterile, Product Code 77500FD - Product Usage: single-use tubing sets used with pump
Hazard: The feeding spike sets may leak at the interface of the tube and spike connector.
November 11, 2020Medical DevicesFDA
Cardinal Health 200, LLC recalls Covidien MONOJECT Standard Hypodermic Needle, Polypropylene Hub 22 G x 3/4". Intended use to facilitate activities such
Hazard: Potential for the needle to detach from the cartridge after the bottom of the cartridge is twisted and removed. If the needle is not securely seated, the needle can fall out of the sheath and cause the unused needle to project out of the cartridge, and result in a needle stick/puncture from the clean/unused needle
October 7, 2020Medical DevicesFDA
Cardinal Health 200, LLC recalls KIT, PRE OP DRAH - Product Usage: Preoperative kit used to decolonize intranasal S. aureus.
Hazard: Only providing one nasal swab in our pre-operative kit instead of the 4 required for proper treatment.
September 9, 2020Medical DevicesFDA
Cardinal Health 200, LLC recalls PROTEXIS Latex Micro Surgical Gloves Size 9.0 - Product Usage: This surgeon s glove is a disposable device made of natur
Hazard: A degradation defect was found that could lead to holes and donning tears at the folding area around the cuffs.
September 9, 2020Medical DevicesFDA
Cardinal Health 200, LLC recalls PROTEXIS Latex Micro Surgical Gloves Size 8.5 - Product Usage: This surgeon s glove is a disposable device made of natur
Hazard: A degradation defect was found that could lead to holes and donning tears at the folding area around the cuffs.
September 9, 2020Medical DevicesFDA
Cardinal Health 200, LLC recalls PROTEXIS Latex Micro Surgical Gloves Size 8.0 - Product Usage: This surgeon s glove is a disposable device made of natur
Hazard: A degradation defect was found that could lead to holes and donning tears at the folding area around the cuffs.
September 9, 2020Medical DevicesFDA
Cardinal Health 200, LLC recalls PROTEXIS Latex Micro Surgical Gloves Size 7.5 - Product Usage: This surgeon s glove is a disposable device made of natur
Hazard: A degradation defect was found that could lead to holes and donning tears at the folding area around the cuffs.
September 9, 2020Medical DevicesFDA
Cardinal Health 200, LLC recalls PROTEXIS Latex Micro Surgical Gloves Size 7.0 - Product Usage: This surgeon s glove is a disposable device made of natur
Hazard: A degradation defect was found that could lead to holes and donning tears at the folding area around the cuffs.
September 9, 2020Medical DevicesFDA
Cardinal Health 200, LLC recalls PROTEXIS Latex Micro Surgical Gloves Size 6.5 - Product Usage: This surgeon s glove is a disposable device made of natur
Hazard: A degradation defect was found that could lead to holes and donning tears at the folding area around the cuffs.
September 9, 2020Medical DevicesFDA
Cardinal Health 200, LLC recalls PROTEXIS Latex Micro Surgical Gloves Size 6.0 - Product Usage: This surgeon s glove is a disposable device made of natur
Hazard: A degradation defect was found that could lead to holes and donning tears at the folding area around the cuffs.
September 9, 2020Medical DevicesFDA
Cardinal Health 200, LLC recalls PROTEXIS Latex Micro Surgical Gloves Size 5.5 - Product Usage: This surgeon s glove is a disposable device made of natur
Hazard: A degradation defect was found that could lead to holes and donning tears at the folding area around the cuffs.
July 15, 2020Medical DevicesFDA
Cardinal Health 200, LLC recalls Cardinal Health NPWT Occlusion Detection Canister 300cc, Prescription Only - Product Usage: The systems are intended for
Hazard: Canisters potentially contain an oversized O-ring that cannot be installed into the mating connector on the device.
July 15, 2020Medical DevicesFDA
Cardinal Health 200, LLC recalls Cardinal Health NPWT Canister with Gel 300cc, Prescription Only - Product Usage: The systems are intended for use on p
Hazard: Canisters potentially contain an oversized O-ring that cannot be installed into the mating connector on the device.
March 18, 2020Medical DevicesFDA
Cardinal Health 200, LLC recalls Monoject Bluntfill with Filter, 18G x 1-1/2" Item Code 11811022F. Used for drawing fluid from a vial - Product Usage: u
Hazard: Non-sterile product was shipped to customers. Product package is labeled as both "STERILE" and "NON-STERILR" ; the product did not undergo sterilization process and is non-sterile. The usage of a needle that is not sterile could result in infection. Firm is not aware of any reports of patient harm.
March 18, 2020Medical DevicesFDA
Cardinal Health 200, LLC recalls Monoject Hypodermic Safety Needle 25G x 5/8" Item Code 1182558 - Product Usage: used for general purpose injection and
Hazard: Non-sterile product was shipped to customers. Product package is labeled as both "STERILE" and "NON-STERILR" ; the product did not undergo sterilization process and is non-sterile. The usage of a needle that is not sterile could result in infection. Firm is not aware of any reports of patient harm.
March 18, 2020Medical DevicesFDA
Cardinal Health 200, LLC recalls Monoject Hypodermic Safety Needle 30G X 1/2" Item Code 1183005 - Product Usage: used for general purpose injection and a
Hazard: Non-sterile product was shipped to customers. Product package is labeled as both "STERILE" and "NON-STERILR" ; the product did not undergo sterilization process and is non-sterile. The usage of a needle that is not sterile could result in infection. Firm is not aware of any reports of patient harm.
March 18, 2020Medical DevicesFDA
Cardinal Health 200, LLC recalls Monoject 3mL Syringe with Hypodermic Safety Needle, 22G x 1-1/2 . Item Code 11832215 - Product Usage: used for general p
Hazard: Non-sterile product was shipped to customers. Product package is labeled as both "STERILE" and "NON-STERILR" ; the product did not undergo sterilization process and is non-sterile. The usage of a needle that is not sterile could result in infection. Firm is not aware of any reports of patient harm.
February 26, 2020Medical DevicesFDA
Cardinal Health 200, LLC recalls Presource Procedure Packs containing AAMI Level 3 surgical gowns, Multiple Catalog Numbers Produced Between September 1,
Hazard: The kits contained recalled surgical gowns. The gowns were manufactured at locations that did not maintain proper environmental conditions. There is no assurance that the surgical gowns are sterile. An inadequately sterilized surgical gown could compromise a sterile field and increase the risk of a surgical site infection.
February 26, 2020Medical DevicesFDA
Cardinal Health 200, LLC recalls Presource Procedure Packs containing AAMI Level 3 surgical gowns, Multiple Catalog Numbers Produced Between September 1,
Hazard: The kits contained recalled surgical gowns. The gowns were manufactured at locations that did not maintain proper environmental conditions. There is no assurance that the surgical gowns are sterile. An inadequately sterilized surgical gown could compromise a sterile field and increase the risk of a surgical site infection.
February 12, 2020Medical DevicesFDA
Cardinal Health 200, LLC recalls Genius 2 Tympanic Thermometer Private Label Item Code: 3069
Hazard: The frequency of calibration for the Genius Tympanic Thermometer as stated in the operating manual may not ensure that thermometers always remain within the stated accuracy range (¿ 0.2¿C for Genius 2 and ¿ 0.3¿C for Genius 3 thermometers). The measurement readings drift upwards over time, which means that the thermometers could exceed the upper stated accuracy tolerance of +0.2¿C for Genius 2 or +0.3¿C for Genius 3.