FoodJul 20, 2022
J & M Foods Favorite Day Lavender Shortbread Cookie Bites Net Wt 7oz recall — FDA F-1414-2022
Undeclared egg and soy lecithin
Class IFDA: TerminatedJ & M Foods, 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 72
Records are ordered by the best available source date.
FoodJul 20, 2022
Bakery Barn 1st Phorm High Quality Protein Level-1 Bar Chocolate Crunch recall — FDA F-1419-2022
Protein bar may be contaminated with plastic and paper foreign material
Class IIFDA: TerminatedBakery Barn, LLC
FoodJul 20, 2022
Premier Research Labs AloePro Dietary Supplement Made With Organic ALOE VERA LIQUID recall — FDA F-1418-2022
Product spoiling over time; spoilage visible beneath lid/closure upon opening.
Class IIFDA: TerminatedPremier Research Labs LLC
DrugJul 20, 2022
Hydrogen Peroxide Topical Solution, USP, 32 fl. oz. (1 QT) 946 mL recall — FDA D-1191-2022
Labeling: Label Mix-Up-The primary label on the front of the bottles have Hydrogen Peroxide affixed to the front and back of the containers. However, the product inside the bottle is 70%…
Class IIFDA: TerminatedVi-Jon, LLC
DrugJul 20, 2022
Bryant Ranch Prepack Morphine Sulfate extended-Release Tablets, USP recall — FDA D-1187-2022
Labeling: Label Mix-up: bottles labeled as Morphine Sulfate 60 mg Extended-Release tablets contain Morphine Sulfate 30 mg Extended-Release tablets and bottles labeled as Morphine Sulfate 30…
Class IFDA: TerminatedBryant Ranch Prepack, Inc.
DrugJul 20, 2022
Latin Foods Market Arti King Refozado con Ortiga y Omega 3 Tablets, 100-count bottles, Hecho recall — FDA D-1284-2022
Marketed Without An Approved NDA/ANDA: FDA laboratory analysis found the product to contain undeclared diclofenac and dexamethasone.
Class IFDA: TerminatedLatin Foods Market
DrugJul 20, 2022
Bryant Ranch Prepack Morphine Sulfate extended-Release Tablets, USP recall — FDA D-1188-2022
Labeling: Label Mix-up: bottles labeled as Morphine Sulfate 60 mg Extended-Release tablets contain Morphine Sulfate 30 mg Extended-Release tablets and bottles labeled as Morphine Sulfate 30…
Class IFDA: TerminatedBryant Ranch Prepack, Inc.
DrugJul 20, 2022
Testosterone Cypionate Injection, USP, 200mg/mL, CIII recall — FDA D-1190-2022
cGMP - Water leakage
Class IIFDA: TerminatedSUN PHARMACEUTICAL INDUSTRIES Inc.
DrugJul 20, 2022
Draximage MAA recall — FDA D-1189-2022
Lack of Assurance of Sterility: Out-of-specification test results obtained for Endotoxin testing.
Class IIFDA: TerminatedJubilant Draximage Inc.
VehicleJul 20, 2022
Volkswagen Group of fuel pump recall — NHTSA campaign 22V516000
Volkswagen Group of America, Inc. (Volkswagen) is recalling certain 2019-2021 Audi Q8, and 2020-2021 Audi Q7 vehicles. A component inside the fuel pump may break, causing the fuel pump to…
fuel pumpVolkswagen Group of America, Inc.
VehicleJul 20, 2022
BMW fuel rail recall — NHTSA campaign 22V513000
BMW of North America, LLC (BMW) is recalling certain 2022 X1 xDrive 28i, X3 xDrive30i, and 228i Gran Coupe vehicles. The high-pressure fuel rail may crack and result in a fuel leak within…
fuel railBMW of North America, LLC
VehicleJul 20, 2022
Volkswagen Group of camera recall — NHTSA campaign 22V514000
Volkswagen Group of America, Inc. (Volkswagen) is recalling certain 2021 Golf GTI, Jetta GLI, Jetta NF, Arteon FL, Tiguan LWB, 2022 Taos, Jetta PA, Tiguan PA, 2021-2022 Atlas Cross Sport,…
cameraVolkswagen Group of America, Inc.
VehicleJul 19, 2022
Kia Motors spare tire recall — NHTSA campaign 22V509000
Kia Motors America (Kia) is recalling certain 2022 Sorento and Telluride vehicles. The vehicles may be equipped with an incorrect spare tire which, when installed, can impair the anti-lock…
spare tireKia Motors America
Medical DeviceJul 13, 2022
Covidien Palindrome HSI Chronic Catheter, Sterile, Single Use, Rx Only recall — FDA Z-1319-2022
There is a potential leaking condition within the hub of specific chronic dialysis catheters, due to an inter-lumen void in the hub component, which may result in unanticipated fluid return…
Class IFDA: OngoingCovidien LLC
Medical DeviceJul 13, 2022
DePuy Spine EIT CIF cage, H 6mm, 8degree, L- an intervertebral body fusion devices indicated recall — FDA Z-1323-2022
Label on the Outer Carton does not match the labels on the Outer Blister package, Inner Blister package and Patient Labels. The only label that may not be correct is on the Outer Carton
Class IIFDA: OngoingDePuy Spine, Inc.
Medical DeviceJul 13, 2022
Siemens Medical Solutions USA syngo Application software VE20 (Material Number 10848815) recall — FDA Z-1339-2022
After CT image data from Toshiba is loaded, image mirroring can occur along the horizontal and vertical image axes. If this error occurs, the patient orientation/position may be…
Class IIFDA: OngoingSiemens Medical Solutions USA, Inc.
Medical DeviceJul 13, 2022
Fresenius Medical Care Holdings NaturaLyte 2301 2K 3.0 Ca 1 Mg Gal, Model No. 08-2301-3 recall — FDA Z-1311-2022
The product was potentially exposed to below-recommended storage temperatures, which may cause leaks in the packaging. Leaks can lead to biological contamination and therefore an increased…
Class IIFDA: TerminatedFresenius Medical Care Holdings, Inc.
Medical DeviceJul 13, 2022
Covidien Palindrome Precision SI Chronic Catheter, Sterile, Single Use, Rx Only recall — FDA Z-1314-2022
There is a potential leaking condition within the hub of specific chronic dialysis catheters, due to an inter-lumen void in the hub component, which may result in unanticipated fluid return…
Class IFDA: OngoingCovidien LLC
Medical DeviceJul 13, 2022
Covidien Palindrome Precision H Chronic Catheter, Sterile, Single Use, Rx Only recall — FDA Z-1313-2022
There is a potential leaking condition within the hub of specific chronic dialysis catheters, due to an inter-lumen void in the hub component, which may result in unanticipated fluid return…
Class IFDA: OngoingCovidien LLC
Medical DeviceJul 13, 2022
Radiometer Medical ApS ABL800 Flex Analyzer Model Numbers 393-800 and 393-801 recall — FDA Z-1321-2022
There is a potential for sporadic incidents of positive and negative biases for analyzer systems configured with cNa+, cCa+, and cK+.
Class IIFDA: OngoingRadiometer Medical ApS
Medical DeviceJul 13, 2022
Covidien Palindrome Chronic Catheter, Sterile, Single Use, Rx Only recall — FDA Z-1316-2022
There is a potential leaking condition within the hub of specific chronic dialysis catheters, due to an inter-lumen void in the hub component, which may result in unanticipated fluid return…
Class IFDA: OngoingCovidien LLC
Medical DeviceJul 13, 2022
Abbott TactiCath Sensor Enabled, Contact Force Ablation Catheter, 8F 115cm FJ, REF A-TCSE-FJ recall — FDA Z-1344-2022
When connected to the EnSite Precision Navigation System, an affected TactiCath Contact Force Ablation Catheter, Sensor Enabled may present the error message: "invalid catheter,, or…
Class IIFDA: TerminatedAbbott
Medical DeviceJul 13, 2022
OSSUR VARIFLEX SUBA JUNIOR foot and ankle external prosthesis, sized for children and recall — FDA Z-1330-2022
Due to receiving complaints related to broken (cracked) prosthetic foot with failures occurring in situations where sudden high impact twisting or bending is applied to the foot.
Class IIFDA: TerminatedOssur Americas
Medical DeviceJul 13, 2022
Luminex Verigene CDF Nucleic Acid Test, Part No. 30-002-22 recall — FDA Z-1334-2022
There is a potential for false negative results using VERIGENE CDF Stool PREP KIT and VERIGENE EP Stool PREP KIT due to hydrophobic characteristics of the swab.
Class IIFDA: OngoingLuminex Corporation
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.