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Consumer Product Recalls
127,277 recalls from the U.S. Consumer Product Safety Commission, newest first.
May 14, 2025Medical DevicesFDA
Galt Medical Corporation recalls GALT Centeze Catheter REF: DRC-002-05 DRC-002-06 The Centeze is intended for use in percutaneous fluid aspirations
Hazard: Due to a potential open seal in the sterile barrier packaging .
May 14, 2025Medical DevicesFDA
Remote Diagnostic Technologies Ltd. recalls Philips Tempus Pro Patient Monitor, REF: 00-1004-R, 00-1007-R, 00-1024-R, 00-1026-R, 00-1004, 00-1007
Hazard: Patient Monitor software update to address issues:1)May freeze at startup with MPM Application error and Attention Restart Required messages,2)Monitor may freeze and reboot at start of 12-lead ECG or after, 3)May reboot after intermittent connection with Smart Mount, 4) 12-lead ECG measurements with Louvain algorithm and software before vx.36 could produce inaccurate rhythm/morphology statements.
May 14, 2025Medical DevicesFDA
Inari Medical - Oak Canyon recalls Artix MT Thrombectomy Device, REF: 32-102
Hazard: Thrombectomy device specifies vessel range of 2.5-6 mm on the pouch, carton, and Instructions for Use rather than the correct vessel range of 3-6 mm, which could incrementally increase the radial force on the artery, which has the potential of vascular complications.
May 14, 2025Medical DevicesFDA
Integra LifeSciences Corp. (NeuroSciences) recalls INSPIRA AIR BALLOON DILATION SYSTEM 10x40, 1 PK. Airway balloon dilation catheter.
Hazard: Incorrect product packaged in INSPIRA AIR Balloon Dilation System carton.
May 14, 2025Medical DevicesFDA
Ambu Inc. recalls Ambu aScope" 5 Broncho HD 5.6/2.8 Sampler Set. Model Number: 622002000US
Hazard: Incorrect labeling in which the front red pouch label did not match the actual size of the medical device. The label on the front of the scope incorrectly states 5.0/2.2 while the back label, shipping box and product inside correctly states 5.6/2.8.
May 14, 2025Medical DevicesFDA
Philips North America Llc recalls Microstream Advance Neonatal-Infant Intubated CO2 Filter Line marketed as Adt/Pedi Intub CO2 Line STerm , Adt/Pedi Intub
Hazard: Disconnection of the adapter from the endotracheal tube can potentially be difficult or not possible.
May 14, 2025Medical DevicesFDA
Getinge Disinfection Ab recalls Washer Disinfector Aquadis 56; Model Number: 56M
Hazard: The frequency inverter is not programmed by supplier according to specification which causes the circulation pump to start earlier than expected, resulting in additional wear and tear, earlier than expected, on the axial seal in the pump housing.
May 14, 2025Medical DevicesFDA
Getinge Disinfection Ab recalls Washer Disinfector Aquadis 56; Model Number: 56A
Hazard: The frequency inverter is not programmed by supplier according to specification which causes the circulation pump to start earlier than expected, resulting in additional wear and tear, earlier than expected, on the axial seal in the pump housing.
May 14, 2025Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Meridian Bioscience ImmunoCard STAT! Crypto/Giardia Test Kits, Model Number 750830
Hazard: A single lot of the ImmunoCard STAT! Crypto/Giardia Test Kit was inadvertently stored in Medline warehouses at temperatures outside of the labeled storage requirements.
May 14, 2025Medical DevicesFDA
SCIENCE & BIO MATERIALS recalls Bio 1 Granules for Filling ¿ 1 mm (2 cm¿), REF:P822692243, Material: BIOSORB (BTCP 95% minimum purity)
Hazard: Vials of implant bone granules may contain less product then specified on labeling.
May 14, 2025Medical DevicesFDA
Integra LifeSciences Corp. (NeuroSciences) recalls CODMAN Craniotomy Kit, Disposable Perforator Cranio-blade Wire Pass Drill, 14mm. Cranial perforator kit.
Hazard: Inadequate weld that can potentially cause the product to disassemble.
May 14, 2025Medical DevicesFDA
Integra LifeSciences Corp. (NeuroSciences) recalls CODMAN Disposable Perforator, 14mm. Cranial perforator.
Hazard: Inadequate weld that can potentially cause the product to disassemble.
May 14, 2025Medical DevicesFDA
Smiths Medical ASD, Inc. recalls CADD Solis VIP Ambulatory Infusion Pump Models: 1) PUMP KIT, CADD-SOLIS VIP, MDL 2120, NA ENGLISH, MANUAL MODE, 1/EA
Hazard: There is a potential for thermal damage in CADD-Solis and CADD- Solis VIP infusion pumps.
May 14, 2025Medical DevicesFDA
Smiths Medical ASD, Inc. recalls CADD-Solis Infusion Pump Models: 1) PUMP KIT, CADD-SOLIS, MDL 2110, V4.2, CE ENGLISH 1/EA, Model Number: 21-2111
Hazard: There is a potential for thermal damage in CADD-Solis and CADD- Solis VIP infusion pumps.
May 14, 2025Medical DevicesFDA
Bausch & Lomb Surgical, Inc. recalls Intraocular Lens. enVista Envy IOL, All models starting with EN; enVista Envy Toric IOL, All models starting with ETN.
Hazard: In response to an increased number of reports of toxic anterior segment syndrome (TASS) in conjunction with implantation of enVista Aspire and enVista Envy IOLs, and certain enVista monofocal lenses in the U.S.
May 14, 2025Medical DevicesFDA
Bausch & Lomb Surgical, Inc. recalls Intraocular lens. enVista Monofocal IOL, All models starting with EE; enVista Aspire IOL, All models starting with EA;
Hazard: In response to an increased number of reports of toxic anterior segment syndrome (TASS) in conjunction with implantation of enVista Aspire and enVista Envy IOLs, and certain enVista monofocal lenses in the U.S.
May 14, 2025Medical DevicesFDA
Smiths Medical ASD, Inc. recalls CADD-Solis VIP Ambulatory Infusion Pump; Model/Number: 21-2120-0100-02 21-2120-0100-03 21-2120-0100-06 21-2120-0
Hazard: Affected pumps may trigger an erroneous (false) Upstream Occlusion Alarm under certain conditions, which will interrupt an active infusion. Interruption or delay of therapy can lead to serious patient injury or death.
May 14, 2025Medical DevicesFDA
Smiths Medical ASD, Inc. recalls CADD-Solis HPCA Ambulatory Infusion Pump; Model/Number: 21-2111-0402-09-KYO 21-2111-0402-09-KYO CADD SOLIS PIB PUMP FO
Hazard: Affected pumps may trigger an erroneous (false) Upstream Occlusion Alarm under certain conditions, which will interrupt an active infusion. Interruption or delay of therapy can lead to serious patient injury or death.
May 14, 2025Medical DevicesFDA
Smiths Medical ASD, Inc. recalls CADD Solis HSPCA Pump ***Updated 5/27/26*** Scope updated to apply specifically to customers using the wireless system.
Hazard: Pumps may experience Wireless Connection Modules intermittent connection alarms, which will interrupt an active infusion. Interruption or delay of therapy can lead to serious patient injury or death.
May 14, 2025Food & BeverageFDA
Taylor Farms Illinois Inc. recalls Trader Joe's Sesame Miso Salad with Salmon, net wt. 10.25oz., in clear plastic clamshell container, UPC 00773164
Hazard: undeclared milk
May 14, 2025Food & BeverageFDA
JJWV Marketing Corporation recalls Ankimo branded Monkfish Liver; NET WT. 7 OZ (200g); Imported and DIST. BY: JJWV Marketing Corporation; Santa Fe Springs,
Hazard: Undeclared allergen ingredient (milk)
May 14, 2025Food & BeverageFDA
Trophy Nut Company recalls Heinen's Honey Roasted Peanuts, NET WT 8.25 OZ (234g), packaged in a composite can with plastic lid, 12 cans per case, B
Hazard: Product mislabeled - product labeled as peanuts, but may contain cashews
May 14, 2025Food & BeverageFDA
Optimal Carnivore, LLC recalls Bone & Joint Restore. 180 capsules in a plastic bottle. Shelf life two years. Store at ambient temperature. Optimal Carn
Hazard: Potential for contamination with salmonella.
May 14, 2025Food & BeverageFDA
LAMB WESTON Inc recalls Item M7422, frozen foodservice Lamb Weston Hashbrown Patties LW Formed Oval 6/3.5LB bags per case. GTIN*10044979922687.
Hazard: Approximately 1mm to 8 mm sized pieces of foreign material (plastic) found in product.
May 14, 2025Food & BeverageFDA
LAMB WESTON Inc recalls Item M7414, frozen foodservice Lamb Weston Hashbrown Patties, frozen, LW Formed Oval 6/3.5LB bags per case. GTIN*1004497
Hazard: Approximately 1mm to 8 mm sized pieces of foreign material (plastic) found in product.
May 14, 2025Food & BeverageFDA
LAMB WESTON Inc recalls Item M0053, frozen foodservice Lamb Weston Hashbrown Patties, frozen, LW Formed Oval 6/3.5LB bags per case. GTIN* 501955
Hazard: Approximately 1mm to 8 mm sized pieces of foreign material (plastic) found in product.
May 14, 2025Food & BeverageFDA
LAMB WESTON Inc recalls Item M7204, frozen foodservice Lamb Weston Hashbrown Patties, frozen, LW Formed Oval 6/3.5LB bags per case. GTIN*1004497
Hazard: Approximately 1mm to 8 mm sized pieces of foreign material (plastic) found in product.
May 14, 2025DrugsFDA
BSO LLC recalls TESTOSTERONE PELLET 200 mg BLUNT, 1 Pellet for Subcutaneous Use, This is a Compounded Drug, Not for Resale, RX or Office
Hazard: Presence of Particulate Matter: Glass particles were found in pellet vials.
May 14, 2025DrugsFDA
BSO LLC recalls TESTOSTERONE PELLET 200 mg (with Cholesterol </=4%), 1 Pellet for Subcutaneous Use, This is a Compounded Drug, Not for R
Hazard: Presence of Particulate Matter: Glass particles were found in pellet vials.
May 14, 2025DrugsFDA
BSO LLC recalls TESTOSTERONE PELLET 200 mg BLUNT (with Cholesterol </=2%), 1 Pellet for Subcutaneous Use, This is a Compounded Drug, Not
Hazard: Presence of Particulate Matter: Glass particles were found in pellet vials.