DrugAug 31, 2022
Midlab Corsair Personal Care 99X Instant Foam Hand Sanitizer recall — FDA D-1464-2022
CGMP Deviations: Product manufactured using expired active ingredient, Benzalkonium chloride.
Class IIFDA: TerminatedMidlab Inc.
Latest records
Latest recalls — page 361
The newest recall records with useful source details are listed here.
DrugAug 31, 2022
Family Dollar Stores, LLC GS ANTI DIARRHEAL LOPERAMIDE CAPLET 12 CT SKU 915632 IMODIUM AD recall — FDA D-1449-2022
CGMP Deviations: product held outside appropriate storage temperature conditions.
Class IIFDA: OngoingFamily Dollar Stores, LLC.
DrugAug 31, 2022
Family Dollar Stores, LLC DOCTOR DANDRUF 2N1 SHAMP CLN APL 13.5FLOZ SKU 2005726 SUAVE 2N1 recall — FDA D-1379-2022
CGMP Deviations: product held outside appropriate storage temperature conditions.
Class IIFDA: OngoingFamily Dollar Stores, LLC.
DrugAug 31, 2022
Family Dollar Stores, LLC DR SCHOLLS ANTI FUNGAL SPRAY PWDER 4.7 OZ SKU 998250 PREMIER recall — FDA D-1375-2022
CGMP Deviations: product held outside appropriate storage temperature conditions.
Class IIFDA: OngoingFamily Dollar Stores, LLC.
DrugAug 31, 2022
Family Dollar Stores, LLC BANANA BOAT SPRT CLR SPRY SPF50 6 FL OZ SKU 2007524 SUNTONE SPORT recall — FDA D-1365-2022
CGMP Deviations: product held outside appropriate storage temperature conditions.
Class IIFDA: OngoingFamily Dollar Stores, LLC.
DrugAug 31, 2022
Family Dollar Stores, LLC QP LAXATIVE BISACODYL 5 MG TABLET 50 CT SKU 902449 QP WOMEN recall — FDA D-1425-2022
CGMP Deviations: product held outside appropriate storage temperature conditions.
Class IIFDA: OngoingFamily Dollar Stores, LLC.
DrugAug 31, 2022
Family Dollar Stores, LLC PEPCID COMPLETE CHEWABLE TAB BERRY 8CT SKU 903365 PEPCID AC recall — FDA D-1419-2022
CGMP Deviations: product held outside appropriate storage temperature conditions.
Class IIFDA: OngoingFamily Dollar Stores, LLC.
DrugAug 31, 2022
Family Dollar Stores, LLC GUARDIAN ANTACID EX STRGTH TBLT FRT 96CT SKU 901379 GUARDIAN recall — FDA D-1414-2022
CGMP Deviations: product held outside appropriate storage temperature conditions.
Class IIFDA: OngoingFamily Dollar Stores, LLC.
DrugAug 31, 2022
Family Dollar Stores, LLC DR SCHOLLS CLR AWAY LIQ WART REMVR 20CT SKU 998384 DR SCHOLLS recall — FDA D-1404-2022
CGMP Deviations: product held outside appropriate storage temperature conditions.
Class IIFDA: OngoingFamily Dollar Stores, LLC.
VehicleAug 31, 2022
Rogue tank recall — NHTSA campaign 22V660000
Nissan North America, Inc. (Nissan) is recalling certain 2022 Rogue vehicles. The fuel tank may have been punctured when vehicle modifications were performed.
tankNissan North America, Inc.
VehicleAug 31, 2022
Volkswagen Group of trailer hitch recall — NHTSA campaign 22V657000
Volkswagen Group of America, Inc. (Volkswagen) is recalling certain 2022 Atlas and Atlas Cross Sport vehicles. The trailer hitch bolts may have been insufficiently tightened.
trailer hitchVolkswagen Group of America, Inc.
VehicleAug 29, 2022
Sportage alternator/generator/regulator recall — NHTSA campaign 22V651000
Kia America, Inc. (Kia) is recalling certain 2023 Sportage vehicles. The alternator battery positive terminal nut may loosen, which can result in an engine stall or an electrical surge.
alternator/generator/regulatorKia America, Inc.
VehicleAug 26, 2022
Chrysler engine control module (ecu/ecm) recall — NHTSA campaign 22V642000
Chrysler (FCA US, LLC) is recalling certain 2022 Ram 3500, 3500 Cab Chassis, Ram 2500, and 4500 and 5500 Cab Chassis vehicles equipped with Cummins 6.7L turbo diesel engines. The engine…
engine control module (ecu/ecm)Chrysler (FCA US, LLC)
VehicleAug 25, 2022
Jeep Gladiator park pawl recall — NHTSA campaign 22V639000
Chrysler (FCA US, LLC) is recalling certain 2022 Jeep Gladiator vehicles. The transmission parking wheel may not properly engage with the parking mechanism.
park pawlChrysler (FCA US, LLC)
VehicleAug 25, 2022
Chrysler display function recall — NHTSA campaign 22V638000
Chrysler (FCA US, LLC) is recalling certain 2020-2021 Jeep Wrangler, RAM 1500 and 2021 Jeep Gladiator vehicles. A radio software error may prevent the rearview image from displaying. As…
display functionChrysler (FCA US, LLC)
DrugAug 24, 2022
Aire-Master of Stage 2-Ophardt Foaming Hand Sanitizer, Fragrance-Free, 1000 mL recall — FDA D-1357-2022
CGMP Deviations: product manufactured using deionized water from a system lacking appropriate microbial control post deionization.
Class IIFDA: TerminatedAire-Master of America Inc.
DrugAug 24, 2022
Aire-Master of Avant Foaming Hand Sanitizer, ethanol 62%, a) 18 fl. oz. bottle (530 mL), b) recall — FDA D-1355-2022
CGMP Deviations: product manufactured using deionized water from a system lacking appropriate microbial control post deionization.
Class IIFDA: TerminatedAire-Master of America Inc.
DrugAug 24, 2022
MEDEK M Hand Sanitizer Ethyl Alcohol Antiseptic 80%v/v, Topical Solution 128 oz/3,785 mL recall — FDA D-1342-2022
Chemical Contamination and Subpotent Drug: FDA analysis found product to contain methanol and below label claim for ethanol.
Class IFDA: TerminatedMEDEK LLC
DrugAug 24, 2022
Acetaminophen Injection, 10 mg/mL, 1,000 mg/100 mL, 100 mL VIAFLO container bag, Single Dose recall — FDA D-1348-2022
Temperature Abuse: Product distributed in refrigerated trucks with labels attached to pallets indicating "Refrigerate Upon Arrival", however product is labeled to be stored in a controlled…
Class IIFDA: TerminatedBaxter Healthcare Corporation
DrugAug 24, 2022
Aire-Master of Avant Foaming Hand Sanitizer Ophardt, Fragrance Free, 1000 mL (33.9 fl. oz.) recall — FDA D-1356-2022
CGMP Deviations: product manufactured using deionized water from a system lacking appropriate microbial control post deionization.
Class IIFDA: TerminatedAire-Master of America Inc.
DrugAug 24, 2022
Nephron Sterile Compounding Center Trisodium Citrate 0.5% Solution, (0.5%/4L), contains Per recall — FDA D-1345-2022
CGMP Deviations: Potential for cross-contamination due to product carryover during manufacturing.
Class IIFDA: TerminatedNephron Sterile Compounding Center LLC
DrugAug 24, 2022
Akron Pharma Acetaminophen 325 mg tablets recall — FDA D-1352-2022
Failed Tablet/Capsule Specifications: Imprint "AP 325" is missing from the tablet.
Class IIIFDA: TerminatedAkron Pharma, Inc.
DrugAug 24, 2022
Zynrelef recall — FDA D-1335-2022
Defective Delivery System: An incorrect 10 mL (12 mL) Luer (slip) syringe packaged in one lot of Zynrelef 400 mg/12 mg kit
Class IIIFDA: TerminatedHERON THERAPEUTICS, Inc.
DrugAug 24, 2022
Nephron Sterile Compounding Center PF-0.125% Bupivacaine HCl Injection, USP, 625 mg/500 mL recall — FDA D-1346-2022
CGMP Deviations: Potential for cross-contamination due to product carryover during manufacturing.
Class IIFDA: TerminatedNephron Sterile Compounding Center LLC
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Recent recall archives
Browse recent months with enough recall history for useful comparison.
August 2026149 records · 4 categoriesJuly 2026371 records · 4 categoriesJune 2026375 records · 4 categoriesMay 2026340 records · 4 categoriesApril 2026415 records · 4 categoriesMarch 2026190 records · 4 categoriesFebruary 2026331 records · 4 categoriesJanuary 2026212 records · 4 categoriesDecember 2025389 records · 4 categoriesNovember 2025326 records · 4 categoriesOctober 2025455 records · 4 categoriesSeptember 2025285 records · 4 categories