DrugJun 1, 2022
Olympia Compounding Pharmacy dba Olympia SB-5 Papaverine 30 mg/mL Phentolamine 3 mg/mL PGE recall — FDA D-0900-2022
Lack of assurance of sterility.
Class IIFDA: CompletedOlympia Compounding Pharmacy dba Olympia Pharmacy
Latest records
Latest recalls — page 371
The newest recall records with useful source details are listed here.
DrugJun 1, 2022
Olympia Compounding Pharmacy dba Olympia Formula F9 Papaverine 0.9 mg/mL Phentolamine 0.1 recall — FDA D-0929-2022
Lack of assurance of sterility.
Class IIFDA: CompletedOlympia Compounding Pharmacy dba Olympia Pharmacy
DrugJun 1, 2022
Eco Lips Higher Education Make Out Ready Vegan Lip Balm, SPF 15, Net Wt. 0.15 oz (4.25 g) recall — FDA D-0890-2022
Mislabeling: The active ingredient list on the label does not match the product's actual ingredients Specifically, the label states Octinoxate 7.5% and Oxybenzone 3%, while the product…
Class IIIFDA: TerminatedEco Lips, Inc.
DrugJun 1, 2022
Tivicay (dolutegravir) Tablets 50 mg, 30-count Bottle recall — FDA D-0896-2022
Labeling: incorrect or missing lot and/or expiration date. An incorrect expiration date was printed on the product labeling with an expiration date of January 2027, whereas the correct…
Class IIIFDA: TerminatedGlaxoSmithKline LLC
DrugJun 1, 2022
Olympia Compounding Pharmacy dba Olympia Lipostat-Plus Methionine 25 mg/mL Inositol 50 mg/mL recall — FDA D-0933-2022
Lack of assurance of sterility.
Class IIFDA: CompletedOlympia Compounding Pharmacy dba Olympia Pharmacy
DrugJun 1, 2022
Calvin Scott & Company Benzphetamine tablets, 50mg, CIII, repackaged in 30-count bottles recall — FDA D-1123-2022
Labeling: Label Mix-up: Bottle labeled as Benzonatate 100 mg capsules contained Benzphetamine 50 mg tablets and a bottle labeled as Benzphetamine 50 mg tablets contained Benzonatate 100 mg…
Class IIIFDA: TerminatedCalvin Scott & Company, Inc.
DrugJun 1, 2022
Olympia Compounding Pharmacy dba Olympia Bimix-3 Papaverine 30 mg/mL Phentolamine 3 mg/mL recall — FDA D-0920-2022
Lack of assurance of sterility.
Class IIFDA: CompletedOlympia Compounding Pharmacy dba Olympia Pharmacy
DrugJun 1, 2022
Olympia Compounding Pharmacy dba Olympia NB-343 Papaverine 30 mg/mL Phentolamine 3 mg/mL PGE recall — FDA D-0940-2022
Lack of assurance of sterility.
Class IIFDA: CompletedOlympia Compounding Pharmacy dba Olympia Pharmacy
DrugJun 1, 2022
Calvin Scott & Company Benzonatate capsules, 100mg, repackaged in 30-count bottles recall — FDA D-1124-2022
Labeling: Label Mix-up: Bottle labeled as Benzonatate 100 mg capsules contained Benzphetamine 50 mg tablets and a bottle labeled as Benzphetamine 50 mg tablets contained Benzonatate 100 mg…
Class IFDA: TerminatedCalvin Scott & Company, Inc.
DrugJun 1, 2022
Olympia Compounding Pharmacy dba Olympia QM-4 Papaverine 30 mg/mL Phentolamine 3 mg/mL recall — FDA D-0897-2022
Lack of assurance of sterility.
Class IIFDA: CompletedOlympia Compounding Pharmacy dba Olympia Pharmacy
DrugJun 1, 2022
Daytrana recall — FDA D-0889-2022
Defective Delivery System: customer complaints exceeded respective action limits.
Class IIFDA: OngoingNoven Pharmaceuticals Inc.
DrugJun 1, 2022
Olympia Compounding Pharmacy dba Olympia T-106 Papaverine 30 mg/mL Phentolamine 1 mg/mL recall — FDA D-0910-2022
Lack of assurance of sterility.
Class IIFDA: CompletedOlympia Compounding Pharmacy dba Olympia Pharmacy
VehicleMay 27, 2022
Mustang control module (tcm/pcm/tecm) recall — NHTSA campaign 22V382000
Ford Motor Company (Ford) is recalling certain 2019-2020 Mustang vehicles equipped with 5.0L engines and manual transmissions. The Powertrain Control Module (PCM) may broadcast an…
control module (tcm/pcm/tecm)Ford Motor Company
VehicleMay 26, 2022
General Motors critical fasteners recall — NHTSA campaign 22V375000
General Motors, LLC (GM) is recalling certain 2022 GMC Canyon and Chevrolet Colorado vehicles equipped with a manual passenger seat. The front passenger seat may have a hook attachment that…
critical fastenersGeneral Motors, LLC
VehicleMay 26, 2022
CR-V tank recall — NHTSA campaign 22V380000
Honda (American Honda Motor Co.) is recalling certain 2020 CR-V vehicles. The clip for the absorber inside the fuel tank was not secured properly and may detach, which can cause an…
tankHonda (American Honda Motor Co.)
DrugMay 25, 2022
Sirolimus Oral Solution, 1 mg/mL, 60 mL bottle recall — FDA D-0881-2022
Failed Dissolution Specifications: Sirolimus Oral Solution recalled due to lot RZ1598 exceeded the specification limit at the 14-month timepoint.
Class IIIFDA: TerminatedApotex Corp.
DrugMay 25, 2022
Plastikon Healthcare MILK OF MAGNESIA USP, (Magnesium Hydroxide), 2400 mg/30 mL, 30 mL cup recall — FDA D-0870-2022
CGMP Deviations: Failure to properly investigate failed microbial testing.
Class IIFDA: CompletedPlastikon Healthcare LLC
DrugMay 25, 2022
Humalog KwikPen, Insulin lispro injection, U-100, 100 units per mL, 5x3 mL Prefilled Pens recall — FDA D-0882-2022
TEMPERATURE ABUSE: Products were exposed to temperatures outside of the products labeled storage conditions due to inclement weather.
Class IFDA: CompletedCardinal Health Inc.
DrugMay 25, 2022
Plastikon Healthcare Magnesium Hydroxide 1200mg, Aluminum Hydroxide 1200mg, Simethicone recall — FDA D-0871-2022
CGMP Deviations: Failure to properly investigate failed microbial testing.
Class IIFDA: CompletedPlastikon Healthcare LLC
DrugMay 25, 2022
Plastikon Healthcare Acetaminophen Oral Solution, USP 650mg/ 20.3 mL cup recall — FDA D-0869-2022
CGMP Deviations: Failure to properly investigate failed microbial testing.
Class IIFDA: CompletedPlastikon Healthcare LLC
DrugMay 25, 2022
Plastikon Healthcare MILK OF MAGNESIA USP, (Magnesium Hydroxide), 2400 mg/30 mL, 30 mL cup recall — FDA D-0867-2022
Microbial Contamination of Non-Sterile Products
Class IFDA: CompletedPlastikon Healthcare LLC
DrugMay 25, 2022
Plastikon Healthcare Magnesium Hydroxide 1200mg, Aluminum Hydroxide 1200mg, Simethicone recall — FDA D-0868-2022
Microbial Contamination of Non-Sterile Products
Class IFDA: CompletedPlastikon Healthcare LLC
DrugMay 25, 2022
Bestco Open Nature Cough Drops Menthol-Cough Suppressant/Oral Anesthetic Peppermint recall — FDA D-0879-2022
Subpotent drug: Low OOS for menthol content at the three month room temperature.
Class IIIFDA: TerminatedBestco LLC
DrugMay 25, 2022
American Health Packaging Nitrofurantoin Capsules, USP recall — FDA D-0880-2022
Failed Dissolution Specifications: Nitrofurantoin Capsules recalled due to dissolution failure at 0-time of the repackaged lot. Drug release results were above specification at 0-time.
Class IIIFDA: TerminatedAmerican Health Packaging
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Recent recall archives
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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