Medical DeviceAug 3, 2022
Medline Custom procedural kits labeled as follows: a recall — FDA Z-1476-2022
Kits contain leaking bottles of isopropyl alcohol
Class IIFDA: OngoingMEDLINE INDUSTRIES, LP - SPT
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 62
Records are ordered by the best available source date.
Medical DeviceAug 3, 2022
Fresenius Medical Care Holdings AquaC UNO H [120V, 60Hz, 1000VA, Fresenius US-Version recall — FDA Z-1464-2022
Internal ethernet cable may be misaligned, the cable jacket (insulation) could become compromised due to high temperature and result in the internal ethernet cable conducting electrical…
Class IIFDA: OngoingFresenius Medical Care Holdings, Inc.
Medical DeviceAug 3, 2022
Intuitive Surgical Da Vinci S/Si Large Clip Applier, Model 420230 Da Vinci S/Si Medium-Large recall — FDA Z-1459-2022
Due to the potential for unexpected motion caused by the partial disengagement of the instrument from the system.
Class IIFDA: OngoingIntuitive Surgical, Inc.
Medical DeviceAug 3, 2022
Abbott Laboratories REF: 08P4320, Alinity c Hemoglobin Reagent Kit, IVD, CE, R1 5 x 46.0 mL recall — FDA Z-1455-2022
There is a potential for falsely elevated Hemoglobin %A1c and Hemoglobin A1c results to be generated using the ARCHITECT and Alinity c Hemoglobin A1c assay.
Class IIFDA: OngoingAbbott Laboratories
Medical DeviceAug 3, 2022
Medline convenience kits: a recall — FDA Z-1471-2022
Kits contain leaking bottles of isopropyl alcohol
Class IIFDA: OngoingMEDLINE INDUSTRIES, LP - SPT
Medical DeviceAug 3, 2022
Abbott Laboratories REF: 4P52-20 Hemoglobin A1c for use with Architect, IVD, CE, R1 1 x 52 recall — FDA Z-1454-2022
There is a potential for falsely elevated Hemoglobin %A1c and Hemoglobin A1c results to be generated using the ARCHITECT and Alinity c Hemoglobin A1c assay.
Class IIFDA: OngoingAbbott Laboratories
Medical DeviceAug 3, 2022
Abbott Laboratories REF: 08P4377, Alinity c Hemoglobin Reagent Kit, IVD, CE, R1 5 x 46.0 mL recall — FDA Z-1456-2022
There is a potential for falsely elevated Hemoglobin %A1c and Hemoglobin A1c results to be generated using the ARCHITECT and Alinity c Hemoglobin A1c assay.
Class IIFDA: OngoingAbbott Laboratories
Medical DeviceAug 3, 2022
Medline Convenience kits labeled as follows: a recall — FDA Z-1470-2022
Kits contain leaking bottles of isopropyl alcohol
Class IIFDA: OngoingMEDLINE INDUSTRIES, LP - SPT
Medical DeviceAug 3, 2022
Sight OLO, Automated Hematology Analyzer, Catalog No recall — FDA Z-1469-2022
The default reference ranges for MCH, MCHC, and RDW for age group "Child 2-11y" are mixed up and incorrectly displayed on OLO devices running software version 2.63, 2.63.1, and 2.63.1.1.…
Class IIFDA: OngoingSIGHT DIAGNOSTICS LTD
Medical DeviceAug 3, 2022
Fresenius Medical Care Holdings AquaC UNO H [120V, 60Hz, 1700VA, Fresenius US-Version recall — FDA Z-1463-2022
Internal ethernet cable may be misaligned, the cable jacket (insulation) could become compromised due to high temperature and result in the internal ethernet cable conducting electrical…
Class IIFDA: OngoingFresenius Medical Care Holdings, Inc.
Medical DeviceAug 3, 2022
GE Healthcare Centricity PACS Software Version 7.0 SP0.0.4.7 recall — FDA Z-1466-2022
The Event Notification Manager (ENM) functionality for certain products does not process notifications for study modifications performed on post verified exams.
Class IIFDA: TerminatedGE Healthcare, LLC
FoodAug 3, 2022
Fuchs Za'atar Seasoning, Cust Part # Lot No recall — FDA F-1507-2022
The product may be potentially positive for Salmonella due to one of the sub-ingredients (oregano) testing positive for Salmonella.
Class IFDA: TerminatedFuchs North America, Inc.
FoodAug 3, 2022
EAT JUST Just Egg Spring Greens Broccoli, Peas, Spinach, Kale, Basil recall — FDA F-1510-2022
Listeria monocytogenes contamination.
Class IIFDA: TerminatedEAT JUST Inc.
FoodAug 3, 2022
Bumble Bee Smoked Clams Shucked Easy Open NET WT recall — FDA F-1508-2022
Detectable levels of Per- and polyfluoroalkyl substances (PFAS).
Class IIFDA: TerminatedBumble Bee Foods, LLC
DrugAug 3, 2022
Eco Lips Juice Beauty, The Organic Solution, SPF 8, Joyful Lip Moisturizer, Hydratant pour recall — FDA D-1298-2022
Failed Dissolution Specifications
Class IIIFDA: TerminatedEco Lips, Inc.
DrugAug 3, 2022
Eco Lips Juice Beauty, The Organic Solution, SPF 8, Naturally Clear Lip Moisturizer recall — FDA D-1299-2022
Failed Dissolution Specifications
Class IIIFDA: TerminatedEco Lips, Inc.
DrugAug 3, 2022
Divalproex Sodium Delayed-Release Tablets, USP 500mg recall — FDA D-1291-2022
Failed Dissolution Specifications: Failure occurred during routine stability testing of dissolution test.
Class IIFDA: TerminatedSUN PHARMACEUTICAL INDUSTRIES Inc.
DrugAug 3, 2022
Propofol Injectable Emulsion, 1 g/100 mL (10 mg/mL) recall — FDA D-1301-2022
Presence of particulate matter: particulate identified as a beetle.
Class IFDA: TerminatedPfizer Inc.
DrugAug 3, 2022
Lansoprazole Delayed-Release Orally Disintegrating Tablets, 35 mg, 100-count blisters per recall — FDA D-1288-2022
FAILED DISSOLUTION SPECIFICATIONS
Class IIFDA: TerminatedDr. Reddy's Laboratories, Inc.
DrugAug 3, 2022
Mylan Pharmaceuticals Insulin Glargine (Insulin glargine-yfgn) Injection, 100 units/mL recall — FDA D-1292-2022
Labeling: Missing label: Label missing from some prefilled pens.
Class IFDA: TerminatedMylan Pharmaceuticals Inc.
DrugAug 3, 2022
Testosterone Gel 1% recall — FDA D-1289-2022
Superpotent Drug: Out of specification assay result was obtained during stability testing.
Class IIFDA: TerminatedTeva Pharmaceuticals USA Inc.
DrugAug 3, 2022
The Procter & Gamble Company Crest 3D White Fluoride Anticavity Toothpaste, Advanced Triple recall — FDA D-1290-2022
Labeling: Missing label: the product tube was missing a label and contained a different formulation.
Class IIIFDA: CompletedThe Procter & Gamble Company
DrugAug 3, 2022
Lansoprazole Delayed-Release Orally Disintegrating Tablets, 15 mg, 100-count blisters per recall — FDA D-1287-2022
FAILED DISSOLUTION SPECIFICATIONS
Class IIFDA: TerminatedDr. Reddy's Laboratories, Inc.
VehicleJul 28, 2022
Chrysler tail lights recall — NHTSA campaign 22V544000
Chrysler (FCA US, LLC) is recalling certain 2022 Jeep Grand Cherokee and 2021-2022 Jeep Grand Cherokee L vehicles. The tail light side marker assemblies may be damaged and not illuminate.…
tail lightsChrysler (FCA US, LLC)
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.