FoodSep 28, 2022
Russ Davis Wholesale Vegetable Tray with Veggie Dip recall — FDA F-1775-2022
Various vegetable and fruit products are recalled due to inadequate sanitizer in wash water.
Class IIFDA: TerminatedRuss Davis Wholesale, LLC
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 40
Records are ordered by the best available source date.
FoodSep 28, 2022
Russ Davis Wholesale Blueberry Salsa recall — FDA F-1776-2022
Various vegetable and fruit products are recalled due to inadequate sanitizer in wash water.
Class IIFDA: TerminatedRuss Davis Wholesale, LLC
FoodSep 28, 2022
Russ Davis Wholesale Sunset Fruit Bowl recall — FDA F-1770-2022
Various vegetable and fruit products are recalled due to inadequate sanitizer in wash water.
Class IIFDA: TerminatedRuss Davis Wholesale, LLC
FoodSep 28, 2022
Russ Davis Wholesale Berry Tray with Fruit Dip containing Strawberry, Blackberry recall — FDA F-1760-2022
Various vegetable and fruit products are recalled due to inadequate sanitizer in wash water.
Class IIFDA: TerminatedRuss Davis Wholesale, LLC
FoodSep 28, 2022
J & N Nut Products Golden Pacific California Shelled Almonds Sliced Almonds 25 recall — FDA F-1746-2022
FDA sampling revealed allergen cross contamination. Almond protein in sliced peanuts and Peanut protein in sliced almonds.
Class IIFDA: TerminatedJ & N Nut Products Inc.
FoodSep 28, 2022
Russ Davis Wholesale Broccoli, Carrot, Strawberry, Red Grape recall — FDA F-1759-2022
Various vegetable and fruit products are recalled due to inadequate sanitizer in wash water.
Class IIFDA: TerminatedRuss Davis Wholesale, LLC
FoodSep 28, 2022
Russ Davis Wholesale Strawberries, Net Wt 5 lb., item # 80309, Keep Refrigerated recall — FDA F-1750-2022
Various vegetable and fruit products are recalled due to inadequate sanitizer in wash water.
Class IIFDA: TerminatedRuss Davis Wholesale, LLC
FoodSep 28, 2022
Russ Davis Wholesale Fruit Medley recall — FDA F-1785-2022
Various vegetable and fruit products are recalled due to inadequate sanitizer in wash water.
Class IIFDA: TerminatedRuss Davis Wholesale, LLC
FoodSep 28, 2022
Russ Davis Wholesale Strawberry & Pineapple recall — FDA F-1755-2022
Various vegetable and fruit products are recalled due to inadequate sanitizer in wash water.
Class IIFDA: TerminatedRuss Davis Wholesale, LLC
FoodSep 28, 2022
Russ Davis Wholesale Roasting Vegetables recall — FDA F-1786-2022
Various vegetable and fruit products are recalled due to inadequate sanitizer in wash water.
Class IIFDA: TerminatedRuss Davis Wholesale, LLC
FoodSep 28, 2022
Russ Davis Wholesale Dragon Fruit Mix recall — FDA F-1784-2022
Various vegetable and fruit products are recalled due to inadequate sanitizer in wash water.
Class IIFDA: TerminatedRuss Davis Wholesale, LLC
DrugSep 28, 2022
Clonidine Hydrochloride Tablets, USP, 0.3 mg, 100-count bottle recall — FDA D-1541-2022
Product mix-up:0.2 mg strength Clonidine Hydrochloride Tablets, USP in a 100-count bottle of 0.3 mg strength Clonidine Hydrochloride Tablets,
Class IIIFDA: TerminatedUNICHEM PHARMACEUTICALS USA Inc.
VehicleSep 26, 2022
Volkswagen Group of hoses, lines/piping, and fittings recall — NHTSA campaign 22V718000
Volkswagen Group of America, Inc. (Volkswagen) is recalling certain 2023 model year Atlas FL and Atlas Cross Sport vehicles. Certain brake lines may leak at the threaded connections.
hoses, lines/piping, and fittingsVolkswagen Group of America, Inc.
VehicleSep 22, 2022
General Motors camera recall — NHTSA campaign 22V709000
General Motors, LLC (GM) is recalling certain 2020-2021 Cadillac XT5, XT6, and GMC Acadia vehicles equipped with the optional Surround Vision feature. The rearview camera coaxial cable…
cameraGeneral Motors, LLC
VehicleSep 22, 2022
General Motors labels recall — NHTSA campaign 22V708000
General Motors, LLC (GM) is recalling certain 2023 Cadillac XT5, XT6, and GMC Acadia vehicles. The certification label located on the driver's side B-pillar contains tire size information…
labelsGeneral Motors, LLC
VehicleSep 22, 2022
Subaru of windshield recall — NHTSA campaign 22V712000
Subaru of America, Inc. (Subaru) is recalling certain 2022 Impreza and Outback vehicles. The incorrect paint clearcoat may have been applied, which can cause the windshield to be…
windshieldSubaru of America, Inc.
Medical DeviceSep 21, 2022
Exactech GXL acetabular liners, orthopedic hip implant component recall — FDA Z-1730-2022
Specific GXL acetabular polyethylene liners, packaged in non-conforming bags, may adversely impact the device and contribute to accelerated wear.
Class IIFDA: OngoingExactech, Inc.
Medical DeviceSep 21, 2022
Cook Roadrunner UniGlide Hydrophilic Wire Guide REFERENCE PART NUMBER (RPN): HPWA-35-80 recall — FDA Z-1714-2022
Product did not meet the acceptance criteria for packaging testing, which included 3-year age acceleration testing, therefore, the sterility of the device may be compromised.
Class IIFDA: OngoingCook Inc.
Medical DeviceSep 21, 2022
Exactech GXL acetabular liners, orthopedic hip implant component recall — FDA Z-1726-2022
Specific GXL acetabular polyethylene liners, packaged in non-conforming bags, may adversely impact the device and contribute to accelerated wear.
Class IIFDA: OngoingExactech, Inc.
Medical DeviceSep 21, 2022
Mako Surgical Stryker USB Converter, Polaris Spectra Camera, Catalog #201148, a component of recall — FDA Z-1735-2022
Certain units have the potential to exhibit infant failures whereby units either arrive non-functional, have the potential to become non-functional, or flash an error light while in use.
Class IIFDA: TerminatedMako Surgical Corporation
Medical DeviceSep 21, 2022
Mallinckrodt, LLC INOmax DSIR -(delivery system) delivers INOMAX recall — FDA Z-1745-2022
The INOmax DSIR Delivery System, manufactured by Mallinckrodt Pharmaceuticals, is not compatible with the upgraded version of the Leoni Plus ventilator, manufactured by Lowenstein Medical.…
Class IIFDA: OngoingMallinckrodt, LLC.
Medical DeviceSep 21, 2022
Cook Roadrunner UniGlide Hydrophilic Wire Guide REFERENCE PART NUMBER (RPN): HPWAS-35-80 recall — FDA Z-1716-2022
Product did not meet the acceptance criteria for packaging testing, which included 3-year age acceleration testing, therefore, the sterility of the device may be compromised.
Class IIFDA: OngoingCook Inc.
Medical DeviceSep 21, 2022
FUJIFILM Healthcare Americas Surpria: Software Version V3.11, V3.22 recall — FDA Z-1749-2022
Error 00003050 or 00003052 may occur during scanning, the captured images will not be reconstructed and the Raw Data will not be displayed in the work list.result, may result in the need…
Class IIFDA: OngoingFUJIFILM Healthcare Americas Corporation
Medical DeviceSep 21, 2022
Cook Roadrunner PC Hydrophilic Wire Guide REFERENCE PART NUMBER (RPN): RFSPC-35-180 ORDER recall — FDA Z-1707-2022
Product did not meet the acceptance criteria for packaging testing, which included 3-year age acceleration testing, therefore, the sterility of the device may be compromised.
Class IIFDA: OngoingCook 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.