Medical DeviceApr 20, 2022
Abbott Vascular 20/30 INDEFLATOR -REF 1000184 WPL2122268-01 (2019-03-01) recall — FDA Z-0921-2022
Due to an increase in complaint trend for leaks and intermittent/loose connections.
Class IIFDA: OngoingAbbott Vascular
Monthly breakdown
2022 recalls by month
Select a month to review the recall records reported during that period.
December 2022318 records · 4 categoriesNovember 2022270 records · 4 categoriesOctober 2022288 records · 4 categoriesSeptember 2022318 records · 4 categoriesAugust 2022293 records · 4 categoriesJuly 2022334 records · 4 categoriesJune 2022348 records · 4 categoriesMay 2022227 records · 4 categoriesApril 2022205 records · 4 categoriesMarch 2022449 records · 4 categoriesFebruary 2022237 records · 4 categoriesJanuary 2022296 records · 4 categories
2022 recalls — page 104
Records are ordered by the best available source date.
Medical DeviceApr 20, 2022
Graphic Controls Acquisition CLARAVUE Pre-wired Electrode - IP SET M3 RT ADULT-US Model recall — FDA Z-0936-2022
Instructions for Use (IFU) (Instructions for Use) indicate compliance with ANSI/AAMI EC53:2013/(R)2020 ECG trunk cables and patient leadwires. Section 5.3.9 of the standard requires the…
Class IIFDA: TerminatedGraphic Controls Acquisition Corporation
Medical DeviceApr 20, 2022
MEDLINE INDUSTRIES, LP - Northfield Stanbio TDM/Beta-Hydroxybutyrate Linearity Standards recall — FDA Z-0933-2022
The product was stored incorrectly due to improper storage controls which may lead to delayed results.
Class IIFDA: TerminatedMEDLINE INDUSTRIES, LP - Northfield
Medical DeviceApr 20, 2022
Breas Ventilator Trolley with the Vivo 50/60/65 and Vivo 45LS ventilator models Article no recall — FDA Z-0943-2022
Ventilator mounting brackets for the Vivo 50/60/65 and Vivo 45LS ventilator models can become detached from the Breas Ventilator Trolley, this may cause the ventilator to fall from the…
Class IIFDA: TerminatedBreas Medical, Inc.
Medical DeviceApr 20, 2022
Sensory Medical Cub 2 Enclosed Bed Canopy System recall — FDA Z-0918-2022
Due potential misuse of the product, firm is updating warnings and precautions booklet for products distributed before December 16, 2021.
Class IFDA: OngoingSensory Medical Inc.
Medical DeviceApr 20, 2022
Nextremity Solutions Nextra Hammertoe Correction System Driver SKU: NX-DR Orthopedic recall — FDA Z-0914-2022
Proximal end of the driver is oversized in varying degrees, making it difficult to fully connect with and remove from the proximal Nextra implant, causing delay in surgery
Class IIFDA: TerminatedNextremity Solutions
Medical DeviceApr 20, 2022
Nextremity Solutions Nextra Hammertoe Correction System 3.5 Middle and 3.2 Proximal Saw Cut recall — FDA Z-0913-2022
Proximal end of the driver is oversized in varying degrees, making it difficult to fully connect with and remove from the proximal Nextra implant, causing delay in surgery
Class IIFDA: TerminatedNextremity Solutions
Medical DeviceApr 20, 2022
Abbott Vascular INDEFLATOR Plus 30 - REF 1000183 WPL2122277-01 (2019-03-01) recall — FDA Z-0924-2022
Due to an increase in complaint trend for leaks and intermittent/loose connections.
Class IIFDA: OngoingAbbott Vascular
Medical DeviceApr 20, 2022
Philips The IFU for the Autoclavable Temperature Probes: Part # 453564635891, providing in recall — FDA Z-0926-2022
Update to instructions for use regarding the cleaning and disinfection process for the reusable probes.
Class IIFDA: OngoingPhilips North America, LLC
Medical DeviceApr 20, 2022
Abbott Vascular Plus 30 Priority Pack w/.096 RHV - REF 1000183 WPL2122277-01 (20-03-01) Plus recall — FDA Z-0925-2022
Due to an increase in complaint trend for leaks and intermittent/loose connections.
Class IIFDA: OngoingAbbott Vascular
Medical DeviceApr 20, 2022
B Braun Medical Conductivity Sensors utilized on Dialog and Dialog+ Hemodialysis Systems recall — FDA Z-0872-2022
Firm learned of the potential for cracks to form in the conductivity sensors during use, which may lead to a leak in the dialysate circuit. This could result in excessive ultrafiltration or…
Class IIFDA: TerminatedB Braun Medical Inc.
Medical DeviceApr 20, 2022
Kaneka LIPOSORBER System, Model: LA-15, consisting of: Apheresis machine, product# 101445 recall — FDA Z-0900-2022
Labeling change to due to the risk of severe anaphylactoid reactions including shock in patients treated with the Liposorber LA-15 LDL Adsorption Column under concomitant ACE inhibitor…
Class IIFDA: TerminatedKaneka America Corp
Medical DeviceApr 20, 2022
Deerfield Imaging Trumpf Mount Clamp Assembly (table adapter component), part #118704-000, a recall — FDA Z-0934-2022
Reports have been received that after normal or routine lateral forces are applied to the head fixation device, the split block clamp may deflect (rotationally around the axis) and not…
Class IIFDA: TerminatedDeerfield Imaging, Inc.
Medical DeviceApr 20, 2022
B Braun Medical Conductivity Sensors utilized on Dialog and Dialog+ Hemodialysis Systems recall — FDA Z-0873-2022
Firm learned of the potential for cracks to form in the conductivity sensors during use, which may lead to a leak in the dialysate circuit. This could result in excessive ultrafiltration or…
Class IIFDA: TerminatedB Braun Medical Inc.
Medical DeviceApr 20, 2022
GE Healthcare MUSE Cardiology Information System, Model Numbers: a) 3101011-040, b) recall — FDA Z-0919-2022
Two scenarios may cause edits to measurements and diagnosis statements can be lost after a test is Signed in the MUSE NX web client.
Class IIFDA: TerminatedGE Healthcare, LLC
FoodApr 20, 2022
B&G Foods Back to Nature Cheddalicious Cheese Flavored Crackers 6 oz recall — FDA F-1005-2022
Undeclared egg and milk due to mispackaging
Class IFDA: TerminatedB&G Foods North America, Inc.
FoodApr 20, 2022
SKIPPY Reduced Fat Creamy Peanut Butter NET WT 40 oz recall — FDA F-0995-2022
Potential to contain small steel contaminants.
Class IIFDA: TerminatedSkippy Foods, LLC.
FoodApr 20, 2022
Taylor Farms - Thai Noodle Salad Kit packaged in 108oz plastic recall — FDA F-0993-2022
Downstream Recall - Foreign Material (Plexiglass) found in ingredient used.
Class IIFDA: TerminatedTaylor Farms
FoodApr 20, 2022
SKIPPY Reduced Fat Chunky Peanut Butter NET WT 16.3 oz recall — FDA F-0996-2022
Potential to contain small steel contaminants.
Class IIFDA: TerminatedSkippy Foods, LLC.
FoodApr 20, 2022
SKIPPY Creamy Peanut Butter Blended with Plant Protein NET WT recall — FDA F-0997-2022
Potential to contain small steel contaminants.
Class IIFDA: TerminatedSkippy Foods, LLC.
FoodApr 20, 2022
Ittella International Tattooed Chef Plant-Based Sausage Breakfast Bowl Frozen recall — FDA F-0992-2022
A gluten free claim was inadvertently used on the lid of the container. However, the ingredient statement declares enriched wheat flour as an ingredient and the allergen information…
Class IIFDA: TerminatedIttella International, LLC
FoodApr 20, 2022
Pepsico Lipton Iced Tea Peach, 24 Pack retail unit, 24 - 16.9 FL OZ recall — FDA F-0982-2022
Immediate package (individual 16.9 FL OZ bottle) is incorrectly labeled as the zero sugar variety, the product inside the bottle is the sugar containing variety
Class IIFDA: TerminatedPepsico Inc.
DrugApr 20, 2022
Preferred Pharmaceuticals Clobetasol Propionate Lotion 0.05%, Generic for Temovate, 118 mL recall — FDA D-0768-2022
CGMP Deviations: all products within expiry are being recalled because the manufacturing firm, Teligent Pharma, Inc. is discontinuing its stability study program.
Class IIFDA: TerminatedPreferred Pharmaceuticals, Inc.
DrugApr 20, 2022
Preferred Pharmaceuticals, Inc recall — FDA D-0769-2022
Out of specification results observed in dissolution during long term stability testing.
Class IIFDA: TerminatedPreferred Pharmaceuticals, Inc.
About the 2022 recall archive
This archive groups records by their reported or recall date. It does not imply that every recall was initiated, announced and resolved during the same calendar year. Open the individual record for the exact dates and source details supplied by FDA or NHTSA.