FoodApr 13, 2022
Top Quality Produce Enoki Mushrooms recall — FDA F-0964-2022
California Department of Public Health tested Enoki mushrooms and had a positive result for Listeria monocytogenes.
Class IFDA: TerminatedTop Quality Produce, Inc.
Latest records
Latest recalls — page 744
The newest recall records with useful source details are listed here.
FoodApr 13, 2022
Fruit Fresh Up All BBD 03/05/22 through 03/23/2022 1 recall — FDA F-0973-2022
may be contaminated with Listeria monocytogenes
Class IFDA: TerminatedFruit Fresh Up, Inc.
FoodApr 13, 2022
T Fresh Company DBA Yes Produce Yes! Enoki Mushrooms recall — FDA F-0962-2022
California Department of Public Health sampled product with a result of Listeria monocytogenes
Class IFDA: TerminatedT Fresh Company DBA Yes Produce
FoodApr 13, 2022
Fruit Fresh Up 1 recall — FDA F-0970-2022
may be contaminated with Listeria monocytogenes
Class IFDA: TerminatedFruit Fresh Up, Inc.
DrugApr 13, 2022
PAPAVERINE HYDROCHLORIDE Injection, USP, 60 mg/2mL (30 mg/mL), packaged as a) 25 x 2mL recall — FDA D-0742-2022
Lack of Assurance of Sterility: deviations from Current Good Manufacturing Practices (CGMP) that call into question the sterility of products intended to be sterile.
Class IIFDA: TerminatedVitae Enim Vitae Scientific, Inc.
DrugApr 13, 2022
DASH Pharmaceuticals Sucralfate Oral Suspension, USP 1g/10mL recall — FDA D-0749-2022
Labeling: Label Mix-Up
Class IIFDA: TerminatedDASH Pharmaceuticals LLC
DrugApr 13, 2022
Cequa recall — FDA D-0770-2022
Subpotent Drug and Presence of Particulate Matter: low out-of-specification results obtained for assay and the presence of particulate matter.
Class IIIFDA: TerminatedSUN PHARMACEUTICAL INDUSTRIES Inc.
DrugApr 13, 2022
Janumet recall — FDA D-0746-2022
Presence of foreign substance: Presence of stainless steel particulates in tablets.
Class IIFDA: TerminatedMERCK SHARP & DOHME CORP
DrugApr 13, 2022
Revive Personal Products Company The Natural Dentist Healthy Breath Antiseptic Rinse, Cool recall — FDA D-0751-2022
Labeling; Label mix-up and Wrong Bar Code; back label incorrectly states active ingredient as Peppermint Oil and Sage Oil and has the wrong UPC
Class IIFDA: TerminatedRevive Personal Products Company
DrugApr 13, 2022
The Ritedose 23.4% Sodium Chloride Injection, 120 mEq per 30 mL (4 mEq/mL), 50 mL prefilled recall — FDA D-0745-2022
Labeling: Incorrect Barcode: Product barcode incorrectly identifies the product as rocuronium bromide injection 100 mg per 10 mL instead of sodium chloride injection 23.4%, 120 mEq per 30…
Class IIIFDA: TerminatedThe Ritedose Corporation
DrugApr 13, 2022
PHENOBARBITAL Sodium Injection, USP, 130 mg/mL, packaged as a) 25 x 1 mL Vials per box recall — FDA D-0744-2022
Lack of Assurance of Sterility: deviations from Current Good Manufacturing Practices (CGMP) that call into question the sterility of products intended to be sterile.
Class IIFDA: TerminatedVitae Enim Vitae Scientific, Inc.
DrugApr 13, 2022
Travoprost Ophthalmic Solution, USP, 0.004%, 2.5 mL bottle recall — FDA D-0748-2022
Subpotent Drug and Failed Impurities/Degradation Specifications: low out-of-specification results obtained for assay and high out-of-specification results for related substance…
Class IIFDA: TerminatedMylan Pharmaceuticals Inc.
DrugApr 13, 2022
PHENOBARBITAL Sodium Injection, USP, 65mg/mL, packaged as a) 25 x 1 mL Vials per box recall — FDA D-0743-2022
Lack of Assurance of Sterility: deviations from Current Good Manufacturing Practices (CGMP) that call into question the sterility of products intended to be sterile.
Class IIFDA: TerminatedVitae Enim Vitae Scientific, Inc.
DrugApr 13, 2022
Adamis Pharmaceuticals SYMJEPI recall — FDA D-0763-2022
Defective Delivery System: Potential clogging of the needle preventing the dispensing of epinephrine.
Class IFDA: TerminatedAdamis Pharmaceuticals Corporation
DrugApr 13, 2022
NETSPOT recall — FDA D-0747-2022
Subpotent Drug: low out-of-specification results for Vial 1 assay obtained during stability studies.
Class IIIFDA: TerminatedAdvanced Accelerator Applications USA, Inc.
DrugApr 13, 2022
Adamis Pharmaceuticals SYMJEPI recall — FDA D-0764-2022
Defective Delivery System: Potential clogging of the needle preventing the dispensing of epinephrine.
Class IFDA: TerminatedAdamis Pharmaceuticals Corporation
DrugApr 13, 2022
Vitae Enim Vitae Scientific TETRACAINE 1% Tetracaine HCI Injection, USP, 20mg/2mL (10mg/mL) recall — FDA D-0741-2022
Lack of Assurance of Sterility: deviations from Current Good Manufacturing Practices (CGMP) that call into question the sterility of products intended to be sterile.
Class IIFDA: TerminatedVitae Enim Vitae Scientific, Inc.
VehicleApr 13, 2022
Sentra headlights recall — NHTSA campaign 22V244000
Nissan North America, Inc. (Nissan) is recalling certain 2020 Sentra vehicles, equipped with LED headlights. The right-hand headlight aim may be misaligned. As such, these vehicles fail to…
headlightsNissan North America, Inc.
VehicleApr 13, 2022
Volkswagen Group of injectors recall — NHTSA campaign 22V245000
Volkswagen Group of America, Inc. (Volkswagen) is recalling certain 2021-2022 Atlas FL and Atlas Cross Sport vehicles. The long fuel injectors may have been assembled without filters.
injectorsVolkswagen Group of America, Inc.
VehicleApr 12, 2022
Tesla electrical system software recall — NHTSA campaign 22V235000
Tesla, Inc. (Tesla) is recalling certain 2020-2022 Model Y, Model X, Model S, and 2017-2022 Model 3 vehicles. The Boombox function allows sounds to be played through an external speaker…
electrical system softwareTesla, Inc.
VehicleApr 8, 2022
Model X curtain recall — NHTSA campaign 22V233000
Tesla, Inc. (Tesla) is recalling certain 2021-2022 Model X vehicles. The left or right front-row side curtain air bags may not deploy as intended when the windows are lowered. As such,…
curtainTesla, Inc.
Medical DeviceApr 6, 2022
Medtronic MiniMed MiniMed 630G: MMT-1715, MMT-1754, MMT-1755 recall — FDA Z-0855-2022
New or replacement insulin pumps are not pre-programmed with basal rates or other verified settings (bolus wizard settings, sensor settings, etc.), which must be set up and saved on pumps…
Class IIFDA: OngoingMedtronic MiniMed
Medical DeviceApr 6, 2022
Illumina NextSeq 550Dx, REF: 20005715, CE, IVD recall — FDA Z-0854-2022
There is a potential that the DNA sequence analyzer may short circuit shortly after disconnection and reconnection of circuit board or imaging module due to an insufficient reconnection of…
Class IIFDA: CompletedIllumina, Inc.
Medical DeviceApr 6, 2022
RaySearch RayStation 4-11B, and RayPlan 1, 2, 7-11B including some service packs: RayStation recall — FDA Z-0850-2022
Incorrect source to skin or surface distance (SSD) calculation may result in dose error when using RayStation system.
Class IIFDA: OngoingRaySearch America Inc.
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Recent recall archives
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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