FoodJan 26, 2022
Aroma Meats Mango Ginger Pickle recall — FDA F-0515-2022
Product was from unapproved source.
Class IIFDA: TerminatedAroma Meats 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 139
Records are ordered by the best available source date.
FoodJan 26, 2022
Aroma Meats Daliya Split Powder recall — FDA F-0512-2022
Product was from unapproved source.
Class IIFDA: TerminatedAroma Meats LLC
FoodJan 26, 2022
Aroma Meats Ginger Pickle recall — FDA F-0517-2022
Product was from unapproved source.
Class IIFDA: TerminatedAroma Meats LLC
FoodJan 26, 2022
Aroma Meats Nethili Pickle is packaged in clear plastic pouch and product recall — FDA F-0508-2022
Fish pickled product is visible and the name Nethili is declared, but anchovy name is not declared on label.
Class IIFDA: TerminatedAroma Meats LLC
DrugJan 26, 2022
Medique Pain-Off recall — FDA D-0390-2022
CGMP Deviations: manufacturer recalled after an FDA inspection noted that these products were not manufactured under Current Good Manufacturing Practices.
Class IIFDA: TerminatedMedique Products
DrugJan 26, 2022
Lohxa SENNA Syrup (sennosides) 8.8 mg/ 5 mL unit-dose cups recall — FDA D-0377-2022
Microbial Contamination of Non-Sterile Product
Class IFDA: TerminatedLohxa, LLC
DrugJan 26, 2022
Dr. Reddy's Laboratories Rite Aid Pharmacy, Allergy & Congestion, Fexofenadine HCl 60mg & recall — FDA D-0380-2022
Failed Dissolution Specifications
Class IIIFDA: TerminatedDr. Reddy's Laboratories, Inc.
DrugJan 26, 2022
Medique Products Extra Strength Headache recall — FDA D-0391-2022
CGMP Deviations: manufacturer recalled after an FDA inspection noted that these products were not manufactured under Current Good Manufacturing Practices.
Class IIFDA: TerminatedMedique Products
DrugJan 26, 2022
Dr. Reddy's Laboratories Dr. Reddys, Fexofenadine HCl 60 mg & Pseudoephedrine HCl 120 mg recall — FDA D-0382-2022
Failed Dissolution Specifications
Class IIIFDA: TerminatedDr. Reddy's Laboratories, Inc.
DrugJan 26, 2022
FEXOFENADINE HCL AND PSEUDOEPHEDRINE HCI Wal-Fex D, Fexofenadine HCl 60mg/Antihistamine & recall — FDA D-0378-2022
Failed Dissolution Specifications
Class IIIFDA: TerminatedDr. Reddy's Laboratories, Inc.
DrugJan 26, 2022
Dr. Reddy's Laboratories Rugby, Antihistamine and Nasal Decongestant, Fexofenadine HCl 60mg recall — FDA D-0379-2022
Failed Dissolution Specifications
Class IIIFDA: TerminatedDr. Reddy's Laboratories, Inc.
DrugJan 26, 2022
Medique Products Physicians CARE Extra Strength PAIN RELIEVER [Acetaminophen, Aspirin recall — FDA D-0389-2022
CGMP Deviations: manufacturer recalled after an FDA inspection noted that these products were not manufactured under Current Good Manufacturing Practices.
Class IIFDA: TerminatedMedique Products
DrugJan 26, 2022
Dr. Reddy's Laboratories equate, Allergy Relief D, Fexofenadine HCl 60mg/Antihistamine recall — FDA D-0383-2022
Failed Dissolution Specifications
Class IIIFDA: TerminatedDr. Reddy's Laboratories, Inc.
DrugJan 26, 2022
Mylan Pharmaceuticals Semglee (insulin glargine) injection, 100 units/mL (U-100), 3 mL recall — FDA D-0462-2022
Labeling: Missing Label: label missing from some Semglee prefilled pens.
Class IFDA: TerminatedMylan Pharmaceuticals Inc.
DrugJan 26, 2022
Dr. Reddy's Laboratories CVS Health, Allergy Relief D, Fexofenadine HCl 60mg/Antihistamine recall — FDA D-0385-2022
Failed Dissolution Specifications
Class IIIFDA: TerminatedDr. Reddy's Laboratories, Inc.
DrugJan 26, 2022
Teva Pharmaceuticals USA Brinzolamide Ophthalmic Suspension, USP 1%, packaged as a)10 ml recall — FDA D-0373-2022
Defective Container: The notch in the cap that fits into the nozzle of the dropper could break off and block the dropper possibly resulting in the product not dispensing.
Class IIFDA: TerminatedTeva Pharmaceuticals USA
DrugJan 26, 2022
Dr. Reddy's Laboratories QC QUALITY CHOICE, Fexofenadine HCl 60mg and Pseudoephedrine HCl recall — FDA D-0384-2022
Failed Dissolution Specifications
Class IIIFDA: TerminatedDr. Reddy's Laboratories, Inc.
VehicleJan 26, 2022
Volkswagen Group of tires recall — NHTSA campaign 22V034000
Volkswagen Group of America, Inc. (Audi) is recalling certain 2019-2021 Audi A5 Sportback, RS5 Coupe, RS5 Sportback, S5 Sportback, 2020-2021 A4 Allroad, A4 Sedan, A5 Cabriolet, A5 Coupe, A6…
tiresVolkswagen Group of America, Inc.
VehicleJan 25, 2022
Kia Motors air bags recall — NHTSA campaign 22V031000
Kia Motors America (Kia) is recalling certain 2017-2019 Sedona, Soul, Soul EV, 2017-2018 Forte, and 2017 Forte Koup vehicles. The Air Bag Control Unit (ACU) cover may contact a memory chip…
air bagsKia Motors America
Medical DeviceJan 19, 2022
DePuy Orthopaedics GLOBAL UNITE STD STEM SZ 8 Part Number: 110008100 recall — FDA Z-0484-2022
Stems may have an undersized spigot bore diameter therefore separating the proximal body from the stem may not be possible without surgical delay and/or bone damage
Class IIFDA: TerminatedDePuy Orthopaedics, Inc.
Medical DeviceJan 19, 2022
DePuy Orthopaedics GLOBAL UNITE STD STEM SZ 6 Part Number: 11000610 recall — FDA Z-0483-2022
Stems may have an undersized spigot bore diameter therefore separating the proximal body from the stem may not be possible without surgical delay and/or bone damage
Class IIFDA: TerminatedDePuy Orthopaedics, Inc.
Medical DeviceJan 19, 2022
Ki Mobility recall — FDA Z-0467-2022
The Instructions for Use provided with the device contained information intended for use of a mechanical wheelchair, not a chair with casters.
Class IIIFDA: TerminatedKi Mobility LLC
Medical DeviceJan 19, 2022
DePuy Orthopaedics GLOBAL UNITE STD STEM SZ 14 Product Code: 110014100 recall — FDA Z-0489-2022
Stems may have an undersized spigot bore diameter therefore separating the proximal body from the stem may not be possible without surgical delay and/or bone damage
Class IIFDA: TerminatedDePuy Orthopaedics, Inc.
Medical DeviceJan 19, 2022
Philips Wireless Footswtich used with the following Philips Allura Xper and Azurion recall — FDA Z-0476-2022
Wireless foot switch connection issues causing interruption of Fluoroscopy and exposure
Class IIFDA: OngoingPhilips North America 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.