DrugAug 24, 2022
Akron Pharma Acetaminophen 500 mg tablet, Extra Strength recall — FDA D-1353-2022
Failed Tablet/Capsule Specifications: Imprint "AP 325" is missing from the tablet.
Class IIIFDA: TerminatedAkron Pharma, Inc.
Latest records
Latest recalls — page 362
The newest recall records with useful source details are listed here.
DrugAug 24, 2022
Aire-Master of Protect U Guard Foaming Hand Sanitizer, Fragrance Free, 18 fl/oz. (530 mL) recall — FDA D-1359-2022
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 Protect U Guard Foaming Hand Sanitizer Ophardt, Fragrance Free, 1000 mL recall — FDA D-1358-2022
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 PF-Labetalol HCl Injection, USP, 20 mg/4 mL (5 mg/mL) recall — FDA D-1347-2022
CGMP Deviations: Potential for cross-contamination due to product carryover during manufacturing.
Class IIFDA: TerminatedNephron Sterile Compounding Center LLC
DrugAug 24, 2022
Nephron Sterile Compounding Center PF-Neostigmine Methylsulfate Injection, USP, 3 mg/3 mL recall — FDA D-1344-2022
CGMP Deviations: Potential for cross-contamination due to product carryover during manufacturing.
Class IIFDA: TerminatedNephron Sterile Compounding Center LLC
DrugAug 24, 2022
Aire-Master of Common Sense Fragrance Free Hand Sanitizer, 250 Gallon Tote, Microbe recall — FDA D-1360-2022
CGMP Deviations: product manufactured using deionized water from a system lacking appropriate microbial control post deionization.
Class IIFDA: TerminatedAire-Master of America Inc.
VehicleAug 18, 2022
Hyundai Motor trailer hitch recall — NHTSA campaign 22V633000
Hyundai Motor America (Hyundai) is recalling 2020-2022 Palisade vehicles potentially equipped with a tow hitch harness installed as original equipment, or purchased as an accessory through…
trailer hitchHyundai Motor America
VehicleAug 18, 2022
Hyundai Motor frontal air bag recall — NHTSA campaign 22V632000
Hyundai Motor America (Hyundai) is recalling certain 2022 Elantra N and 2022-2023 Elantra vehicles. The emblem on the cover of the driver's front air bag may not have been welded properly,…
frontal air bagHyundai Motor America
DrugAug 17, 2022
Telmisartan and Hydrochlorothiazide Tablets USP, 80 mg/12.5 mg, 30 Tablets recall — FDA D-1306-2022
Defective Container: Recall of these batches has been initiated due to complaints of difficult to open blister and tablet breaks while opening the blister .
Class IIFDA: TerminatedGlenmark Pharmaceuticals Inc., USA
DrugAug 17, 2022
SYSTANE LUBRICANT Systane, Lubricant Eye Drops, Polyethylene Glycol 400 0.4% Lubricant recall — FDA D-1314-2022
CGMP Deviations: products were stored outside the drug label specifications.
Class IIFDA: TerminatedMckesson Medical-Surgical Inc. Corporate Office
DrugAug 17, 2022
Lorazepam Injection, USP, 2mg/mL, 1 mL vial, 25 vials per carton recall — FDA D-1307-2022
Failed Impurities/Degradation Specifications: Out-of-specification results observed for total related compounds during testing of retain samples.
Class IIFDA: TerminatedHikma Pharmaceuticals USA Inc.
DrugAug 17, 2022
Naphcon A eye drops, Naphazoline HCl 0.025% and Pheniramine Maleate 0.3%, Redness Reliever recall — FDA D-1313-2022
CGMP Deviations: products were stored outside the drug label specifications.
Class IIFDA: TerminatedMckesson Medical-Surgical Inc. Corporate Office
DrugAug 17, 2022
Telmisartan and Hydrochlorothiazide Tablets USP, 80 mg/25 mg, 30 Tablets recall — FDA D-1305-2022
Defective Container: Recall of these batches has been initiated due to complaints of difficult to open blister and tablet breaks while opening the blister .
Class IIFDA: TerminatedGlenmark Pharmaceuticals Inc., USA
DrugAug 17, 2022
Prednisone Tablets USP, 20 mg, 100-count bottle recall — FDA D-1330-2022
Presence of foreign tablet: 2.5 mg tablet in a 20 mg bottle of Prednisone Tablets
Class IIFDA: TerminatedStrides Pharma Inc.
DrugAug 17, 2022
Lorazepam Injection, USP, 4mg/mL, 1 mL vial, 25 vial per carton recall — FDA D-1310-2022
Failed Impurities/Degradation Specifications: Out-of-specification results observed for total related compounds during testing of retain samples.
Class IIFDA: TerminatedHikma Pharmaceuticals USA Inc.
DrugAug 17, 2022
Mckesson Medical-Surgical Inc. Corporate Office Triple Antibiotic Ointment, Bacitracin zinc recall — FDA D-1311-2022
CGMP Deviations: products were stored outside the drug label specifications.
Class IIFDA: TerminatedMckesson Medical-Surgical Inc. Corporate Office
DrugAug 17, 2022
DAKINS QUARTER Dakin's Solution, a) sodium hypochlorite 0.125%, quarter strength, NDC recall — FDA D-1323-2022
CGMP Deviations: products were stored outside the drug label specifications.
Class IIFDA: TerminatedMckesson Medical-Surgical Inc. Corporate Office
DrugAug 17, 2022
Lorazepam Injection, USP, 2mg/mL, 1 mL vial, 25 vial per carton recall — FDA D-1309-2022
Failed Impurities/Degradation Specifications: Out-of-specification results observed for total related compounds during testing of retain samples.
Class IIFDA: TerminatedHikma Pharmaceuticals USA Inc.
DrugAug 17, 2022
Mckesson Medical-Surgical Inc. Corporate Office Asthmanefrin Racephinephrine Inhalation recall — FDA D-1324-2022
CGMP Deviations: products were stored outside the drug label specifications.
Class IIFDA: TerminatedMckesson Medical-Surgical Inc. Corporate Office
DrugAug 17, 2022
S2 Racepinephrine Inhalation Solution, USP 2.25%, Bronchodilator, For Oral Inhalation Only recall — FDA D-1325-2022
CGMP Deviations: products were stored outside the drug label specifications.
Class IIFDA: TerminatedMckesson Medical-Surgical Inc. Corporate Office
DrugAug 17, 2022
Ativan Injection (lorazepam injection, USP), 2mg/mL, 1 mL vial, 25 vials per carton recall — FDA D-1308-2022
Failed Impurities/Degradation Specifications: Out-of-specification results observed for total related compounds during testing of retain samples.
Class IIFDA: TerminatedHikma Pharmaceuticals USA Inc.
DrugAug 17, 2022
PATADAY ONCE DAILY RELIEF Pataday, Once Daily Relief, Olopatadine hydrochloride ophthalmic recall — FDA D-1321-2022
CGMP Deviations: products were stored outside the drug label specifications.
Class IIFDA: TerminatedMckesson Medical-Surgical Inc. Corporate Office
DrugAug 17, 2022
ZADITOR Systane Zaditor, ketotifen fumarate ophthalmic solution 0.035%, Antihistamine eye recall — FDA D-1317-2022
CGMP Deviations: products were stored outside the drug label specifications.
Class IIFDA: TerminatedMckesson Medical-Surgical Inc. Corporate Office
VehicleAug 15, 2022
Telluride trailer hitch recall — NHTSA campaign 22V626000
Kia America, Inc. (Kia) is recalling certain 2020-2022 Telluride vehicles potentially equipped with a Genuine Kia 4-pin tow hitch harness installed as original equipment, or purchased as an…
trailer hitchKia America, Inc.
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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