FoodDec 7, 2022
fayeon distributors Choi Heong Yuen Bakery Almond Cakes in round metal container recall — FDA F-0182-2023
Product may contain undeclared milk
Class IFDA: Terminatedfayeon distributors Inc.
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 14
Records are ordered by the best available source date.
FoodDec 7, 2022
Perfect Day Coolhaus Dairy Free Cookie Dough Lyfe Frozen Dessert Sandwich recall — FDA F-0179-2023
Presence of coliform found in 3rd party lab samples
Class IIIFDA: TerminatedPerfect Day Inc.
FoodDec 7, 2022
Amys Kitchen Amy's Kitchen Gluten Free Bean and Cheese Burrito 5.5 oz recall — FDA F-0180-2023
Product may contain foreign material: pieces of plastic
Class IIFDA: TerminatedAmys Kitchen Inc.
DrugDec 7, 2022
Daytrana recall — FDA D-0071-2023
Defective Delivery System: Recalled lot was found to be out of specification for shear. Shear is an attribute related to the adhesive properties of the transdermal patches.
Class IIFDA: OngoingNoven Pharmaceuticals Inc.
DrugDec 7, 2022
Acella Pharmaceuticals Sodium Sulfacetamide 10% Sulfur 4% Cleansing Pads, Net weight 3.7g recall — FDA D-0074-2023
Subpotent drug: Out of specification for assay at the end-of-shelf-life 24-month period.
Class IIIFDA: TerminatedAcella Pharmaceuticals, LLC
VehicleDec 6, 2022
Model Y subframe/mounting bracket recall — NHTSA campaign 22V895000
Tesla, Inc. (Tesla) is recalling certain 2023 Model Y vehicles. The front suspension lateral link fasteners may not have been properly attached to the sub-frame.
subframe/mounting bracketTesla, Inc.
Medical DeviceNov 30, 2022
3M Healthcare Business 3M Steri-Drape, Small Towel Drape, REF 1000, general surgery drape recall — FDA Z-0247-2023
During a recent investigation, 3M confirmed the liner on the adhesive component of the affected drapes is difficult to remove without damaging the product and may render the product…
Class IIFDA: Ongoing3M Healthcare Business
Medical DeviceNov 30, 2022
3M Healthcare Business 3M Steri-Drape, Small Drape with Adhesive Aperture, REF 1020NS recall — FDA Z-0254-2023
During a recent investigation, 3M confirmed the liner on the adhesive component of the affected drapes is difficult to remove without damaging the product and may render the product…
Class IIFDA: Ongoing3M Healthcare Business
Medical DeviceNov 30, 2022
3M Healthcare Business 3M Steri-Drape, Medium Drape with Incise Film and Pouch, REF 1061 recall — FDA Z-0262-2023
During a recent investigation, 3M confirmed the liner on the adhesive component of the affected drapes is difficult to remove without damaging the product and may render the product…
Class IIFDA: Ongoing3M Healthcare Business
Medical DeviceNov 30, 2022
3M Healthcare Business 3M Steri-Drape, Medium Drape with Incise Film and Pouch, REF 1061NS recall — FDA Z-0263-2023
During a recent investigation, 3M confirmed the liner on the adhesive component of the affected drapes is difficult to remove without damaging the product and may render the product…
Class IIFDA: Ongoing3M Healthcare Business
Medical DeviceNov 30, 2022
PAJUNK Continuous Epidural Tray, Tuohy Epidural Needle 17G x 4" with EpiLong Soft Catheter recall — FDA Z-0278-2023
The tray contains a 2ml ampule of 0.75% Marcaine Spinal in lieu of a 10ml ampule of 0.9% Sodium Chloride as intended,.
Class IIFDA: TerminatedPajunk Medical Systems, L.P.
Medical DeviceNov 30, 2022
Hamilton Medical AG Hamilton-C6 recall — FDA Z-0267-2023
Due to a malfunction related to the backlight on the ventilator screen. The screen goes black for approximately 2-3 seconds, but it brightens up again when the backlight switches on again.
Class IIFDA: OngoingHamilton Medical AG
Medical DeviceNov 30, 2022
Southmedic SAFETY CARTRIDGE WITH SOUTHMEDIC PLUS SURGICAL BLADE, REF 73-8020, STERILE EO recall — FDA Z-0279-2023
Upon review of its batch record, Southmedic identified that lot # W92761 was not sent out for sterilization, and was instead transferred directly to distribution where it was sold and…
Class IIFDA: OngoingSouthmedic, Inc.
Medical DeviceNov 30, 2022
3M Healthcare Business 3M Steri-Drape, Medium Drape with Adhesive Aperture, REF 1030 recall — FDA Z-0257-2023
During a recent investigation, 3M confirmed the liner on the adhesive component of the affected drapes is difficult to remove without damaging the product and may render the product…
Class IIFDA: Ongoing3M Healthcare Business
Medical DeviceNov 30, 2022
Corin Unity Total Knee System recall — FDA Z-0273-2023
The internal packaging system for devices may have damage to the blisters potentially damaging the device or compromising the sterility of the packaging.
Class IIFDA: TerminatedCorin Ltd
Medical DeviceNov 30, 2022
3M Healthcare Business 3M Steri-Drape, Small Drape with Incise Film, REF 1021, general recall — FDA Z-0255-2023
During a recent investigation, 3M confirmed the liner on the adhesive component of the affected drapes is difficult to remove without damaging the product and may render the product…
Class IIFDA: Ongoing3M Healthcare Business
Medical DeviceNov 30, 2022
3M Healthcare Business 3M Steri-Drape, Small Towel Drape, REF 1000NS, general surgery drape recall — FDA Z-0248-2023
During a recent investigation, 3M confirmed the liner on the adhesive component of the affected drapes is difficult to remove without damaging the product and may render the product…
Class IIFDA: Ongoing3M Healthcare Business
Medical DeviceNov 30, 2022
3M Healthcare Business 3M Steri-Drape, Small Drape with Incise Film, REF 1021NS, general recall — FDA Z-0256-2023
During a recent investigation, 3M confirmed the liner on the adhesive component of the affected drapes is difficult to remove without damaging the product and may render the product…
Class IIFDA: Ongoing3M Healthcare Business
Medical DeviceNov 30, 2022
3M Healthcare Business 3M Steri-Drape, Medium Drape with Incise Film, REF 1060NS, general recall — FDA Z-0261-2023
During a recent investigation, 3M confirmed the liner on the adhesive component of the affected drapes is difficult to remove without damaging the product and may render the product…
Class IIFDA: Ongoing3M Healthcare Business
Medical DeviceNov 30, 2022
3M Healthcare Business 3M Steri-Drape, Large Towel Drape, REF 1010NS, general surgery drape recall — FDA Z-0251-2023
During a recent investigation, 3M confirmed the liner on the adhesive component of the affected drapes is difficult to remove without damaging the product and may render the product…
Class IIFDA: Ongoing3M Healthcare Business
Medical DeviceNov 30, 2022
3M Healthcare Business 3M Steri-Drape, Medium Drape with Adhesive Aperture, REF 1030NS recall — FDA Z-0258-2023
During a recent investigation, 3M confirmed the liner on the adhesive component of the affected drapes is difficult to remove without damaging the product and may render the product…
Class IIFDA: Ongoing3M Healthcare Business
Medical DeviceNov 30, 2022
3M Healthcare Business 3M Steri-Drape, Medium Drape with Wide Adhesive Aperture, REF 1033 recall — FDA Z-0259-2023
During a recent investigation, 3M confirmed the liner on the adhesive component of the affected drapes is difficult to remove without damaging the product and may render the product…
Class IIFDA: Ongoing3M Healthcare Business
Medical DeviceNov 30, 2022
3M Healthcare Business 3M Steri-Drape, Large Towel Drape, REF 1010NSD, general surgery drape recall — FDA Z-0252-2023
During a recent investigation, 3M confirmed the liner on the adhesive component of the affected drapes is difficult to remove without damaging the product and may render the product…
Class IIFDA: Ongoing3M Healthcare Business
Medical DeviceNov 30, 2022
Abbott Molecular Alinity m System, REF 08N53-002, For In Vitro Diagnostic Use recall — FDA Z-0268-2023
Abbott has identified potential performance issues for the Alinity m System software version 1.6.5: 1) In a unique scenario, the waste chute flapper was found to not open when the Systems…
Class IIFDA: OngoingAbbott Molecular, 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.