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
Latest records
Latest recalls — page 728
The newest recall records with useful source details are listed here.
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.)
Medical DeviceMay 25, 2022
Beckman Coulter MicroScan WalkAway-96 plus Instrument REF B1018-284 recall — FDA Z-1084-2022
WalkAway Instruments may have been assembled with the incorrect AC power entry connector inlet with is rated at 1 ampere current rating rather than the correct current rating of 10 ampere
Class IIFDA: OngoingBeckman Coulter Inc.
Medical DeviceMay 25, 2022
Abbott Vascular Dragonfly OpStar Imaging Catheter, REF 1014651/1014652, 0.068 in, 0.014 in recall — FDA Z-1095-2022
There is a potential that the proximal marker may separate from the imaging catheter
Class IFDA: OngoingAbbott Vascular
Medical DeviceMay 25, 2022
Windstone Medical Packaging Prevantics swabs and/or swabsticks contained inside the recall — FDA Z-1101-2022
Convenience kits contain one or more swab/swabstick drug products, manufactured by Professional Disposables International, that are subject to a drug recall due to uncertainty of the…
Class IIFDA: OngoingWindstone Medical Packaging, Inc.
Medical DeviceMay 25, 2022
Beckman Coulter MicroScan WalkAway-96 plus Reconditioned Instrument REF B1018-396R recall — FDA Z-1088-2022
WalkAway Instruments may have been assembled with the incorrect AC power entry connector inlet with is rated at 1 ampere current rating rather than the correct current rating of 10 ampere
Class IIFDA: OngoingBeckman Coulter Inc.
Medical DeviceMay 25, 2022
Boston Scientific EXALT Model D Single-Use Duodenoscope (Box 2) UPN: M0054242CE1 Intended recall — FDA Z-1082-2022
Updated Instructions for Use (IFU) for EXALT Model D Single-Use Duodenoscope highlight the known risk of perforation and provide best clinical practices related to insertion, advancement,…
Class IIFDA: OngoingBoston Scientific Corporation
Medical DeviceMay 25, 2022
Medtronic Instructions for Use, Patient Manuals, and Emergency Responder Guides for recall — FDA Z-1110-2022
Errors and inconsistencies that were identified in the Instruction for Use (IFU), Emergency Responder Guide (ERG), and Patient Manual (PM) for the HeartWare Ventricular Assist Device (HVAD)…
Class IIFDA: OngoingMedtronic Inc.
Medical DeviceMay 25, 2022
Total Resources International First Aid Kits, Item Numbers: 10HBC01087, 10HBC01092A3PK recall — FDA Z-1089-2022
ULTRAtab Laboratories recalled Acetaminophen and electrolyte tablets that were later placed into Total Resources Intl kits. Acetaminophen and electrolyte tablets were recalled due to a…
Class IIFDA: TerminatedTotal Resources Intl
Medical DeviceMay 25, 2022
Smith & Nephew LEGION NARROW PS OXIN SZ 6N RT and JRNY II BCS FEMORAL OXIN LT SZ 5 recall — FDA Z-1099-2022
It was reported that a JOURNEY II BCS Femoral OXIN LT SZ5 was in a box labelled as a LEGION NARROW PS OXIN SZ 6N RT.
Class IIFDA: TerminatedSmith & Nephew Inc.
Medical DeviceMay 25, 2022
CooperSurgical VITRIGUARD, CARRIER, CLEAR recall — FDA Z-1108-2022
Products in this lot may have compromised barrier seals, introducing a risk to sterility.
Class IIFDA: OngoingCooperSurgical, Inc.
Medical DeviceMay 25, 2022
Neuralynx ATLAS Stim Headbox-NK For use only with the ATLAS Neurophysiology System recall — FDA Z-1091-2022
Atlas Stim Headbox (ASHB) was delivered to US customers under a premise that the device had an Investigational Device Exemption (IDE) and was for research use only, but the manufacturer…
Class IIFDA: OngoingNeuralynx Inc.
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Recent recall archives
Browse recent months with enough recall history for useful comparison.
October 2026110 records · 3 categoriesSeptember 2026364 records · 4 categoriesAugust 2026302 records · 4 categoriesJuly 2026370 records · 4 categoriesJune 2026376 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 categories