DrugApr 21, 2021
Spartan Chemical Co Lite'n Foamy Lemon Blossom Hand Sanitizer recall — FDA D-0359-2021
Microbial Contamination of Non-Sterile Products; lot tested positive for Bulkholderia multivorans
Class IFDA: TerminatedSpartan Chemical Co Inc.
Latest records
Latest recalls — page 883
The newest recall records with useful source details are listed here.
DrugApr 21, 2021
Antiseptic Hand Cleaner (Chloroxylenol, 1.0%), Net Contents: 1 US Gallon/ 3.79 Liters per recall — FDA D-0361-2021
CGMP Deviations
Class IIFDA: TerminatedSpartan Chemical Co Inc.
DrugApr 21, 2021
INSULIN DILUTING MEDIUM FOR NOVOLOG NovoLog (Insulin aspart) Injection, 100 units/mL recall — FDA D-0616-2021
Temperature Abuse: product samples were stored at temperatures below 32* F which is not in accordance with storage requirements that could cause a lack of efficacy and damage to the…
Class IFDA: TerminatedNovo Nordisk Inc.
DrugApr 21, 2021
TRESIBA FlexTouch recall — FDA D-0619-2021
Temperature Abuse: product samples were stored at temperatures below 32* F which is not in accordance with storage requirements that could cause a lack of efficacy and damage to the…
Class IFDA: TerminatedNovo Nordisk Inc.
DrugApr 21, 2021
LITE NFOAMY HEALTHCARE PERSONNEL HANDWASH Lite'n Foamy Healthcare Personnel Handwash recall — FDA D-0364-2021
CGMP Deviations
Class IIFDA: TerminatedSpartan Chemical Co Inc.
DrugApr 21, 2021
LITE NFOAMY E2 SANITIZING HANDWASH Lite'n Foamy E2 Sanitizing Handwash recall — FDA D-0362-2021
CGMP Deviations
Class IIFDA: TerminatedSpartan Chemical Co Inc.
DrugApr 21, 2021
Fiasp FlexTouch (insulin aspart injection) 100 units/mL (U-100), 3 mL Prefilled Pen, Sample recall — FDA D-0611-2021
Temperature Abuse: product samples were stored at temperatures below 32* F which is not in accordance with storage requirements that could cause a lack of efficacy and damage to the…
Class IFDA: TerminatedNovo Nordisk Inc.
DrugApr 21, 2021
Fiasp (insulin aspart injection), 100 units/mL (U-100), One 10 mL multi-dose vial, Sample recall — FDA D-0613-2021
Temperature Abuse: product samples were stored at temperatures below 32* F which is not in accordance with storage requirements that could cause a lack of efficacy and damage to the…
Class IFDA: TerminatedNovo Nordisk Inc.
DrugApr 21, 2021
Levemir FlexTouch (insulin detemir) injection, 100 units/mL (U-100), 3 mL Prefilled Pen recall — FDA D-0614-2021
Temperature Abuse: product samples were stored at temperatures below 32* F which is not in accordance with storage requirements that could cause a lack of efficacy and damage to the…
Class IFDA: TerminatedNovo Nordisk Inc.
DrugApr 21, 2021
Xultophy 100/3.6 recall — FDA D-0623-2021
Temperature Abuse: product samples were stored at temperatures below 32* F which is not in accordance with storage requirements that could cause a lack of efficacy and damage to the…
Class IFDA: TerminatedNovo Nordisk Inc.
DrugApr 21, 2021
Cefprozil for Oral Suspension USP, 250mg/5mL, packaged as a) 50 mL (when mixed) bottles recall — FDA D-0332-2021
Superpotent Drug
Class IIFDA: TerminatedLupin Pharmaceuticals Inc.
DrugApr 21, 2021
Fiasp PenFill (insulin aspart injection) 100 units/mL (U-100), 3 mL cartridge, 5 cartridges recall — FDA D-0612-2021
Temperature Abuse: product samples were stored at temperatures below 32* F which is not in accordance with storage requirements that could cause a lack of efficacy and damage to the…
Class IFDA: TerminatedNovo Nordisk Inc.
DrugApr 21, 2021
TRESIBA recall — FDA D-0620-2021
Temperature Abuse: product samples were stored at temperatures below 32* F which is not in accordance with storage requirements that could cause a lack of efficacy and damage to the…
Class IFDA: TerminatedNovo Nordisk Inc.
DrugApr 21, 2021
Riomet recall — FDA D-0334-2021
Microbial Contamination of Non-Sterile Product
Class IIFDA: TerminatedSUN PHARMACEUTICAL INDUSTRIES Inc.
DrugApr 21, 2021
ViCTOZA (liraglutide) injection, 18 mg/3 mL (6 mg/mL), contains: 1 Victoza Pen, Sample Not recall — FDA D-0622-2021
Temperature Abuse: product samples were stored at temperatures below 32* F which is not in accordance with storage requirements that could cause a lack of efficacy and damage to the…
Class IIFDA: TerminatedNovo Nordisk Inc.
DrugApr 21, 2021
Novo Nordisk OZEMPIC (semaglutide) injection, 2 mg/1.5 mL (1.34 mg/mL) Prefilled pen, 1 pen recall — FDA D-0617-2021
Temperature Abuse: product samples were stored at temperatures below 32* F which is not in accordance with storage requirements that could cause a lack of efficacy and damage to the…
Class IIFDA: TerminatedNovo Nordisk Inc.
DrugApr 21, 2021
Asclemed USA Inc. dba Enovachem Pharmaceuticals Distributed by: DocRx, Methylprednisolone recall — FDA D-0330-2021
Labeling: Illegible label: Manufacturer received complaint of mis-alignment print of the printed dosing instructions on the blister card.
Class IIIFDA: OngoingAsclemed USA Inc. dba Enovachem Pharmaceuticals
DrugApr 21, 2021
Spartan Chemical Co foamyiQ Lemon Blossom Hand Sanitizer recall — FDA D-0360-2021
CGMP Deviations
Class IIFDA: TerminatedSpartan Chemical Co Inc.
DrugApr 21, 2021
INSULIN DILUTING MEDIUM FOR NOVOLOG NovoLog FlexPen (insulin aspart) Injection, 100 recall — FDA D-0615-2021
Temperature Abuse: product samples were stored at temperatures below 32* F which is not in accordance with storage requirements that could cause a lack of efficacy and damage to the…
Class IFDA: TerminatedNovo Nordisk Inc.
DrugApr 21, 2021
Saxenda (liraglutide) Injection, 18 mg/3 mL (6 mg/mL), 1 x 3 mL Prefilled Pen, Sample recall — FDA D-0618-2021
Temperature Abuse: product samples were stored at temperatures below 32* F which is not in accordance with storage requirements that could cause a lack of efficacy and damage to the…
Class IIFDA: TerminatedNovo Nordisk Inc.
VehicleApr 21, 2021
XC90 Excellence electrical system software recall — NHTSA campaign 21V273000
Volvo Car USA, LLC (Volvo Car) is recalling certain 2016-2020 XC90 Excellence vehicles. Liquid or condensation on the rear seat control display may cause the front passenger seat to move…
electrical system softwareVolvo Car USA, LLC
VehicleApr 15, 2021
Subaru of electrical system software recall — NHTSA campaign 21V264000
Subaru of America, Inc. (Subaru) is recalling certain 2017-2019 Subaru Impreza and 2018-2019 Crosstrek vehicles. The Engine Control Module (ECM) may continue to power the ignition coil…
electrical system softwareSubaru of America, Inc.
VehicleApr 15, 2021
Subaru of rear recall — NHTSA campaign 21V263000
Subaru of America, Inc. (Subaru) is recalling certain 2018-2019 Subaru Crosstrek, 2019 Crosstrek Hybrid, and 2019 Forester vehicles. The rear stabilizer bracket bolts may loosen and detach.
rearSubaru of America, Inc.
Medical DeviceApr 14, 2021
Fujifilm Medical Systems U.S.A Synapse PACS - Radiological Image Processing System - Product recall — FDA Z-1348-2021
The wrong patient information may be displayed in the viewer or PowerJacket.
Class IIFDA: OngoingFujifilm Medical Systems U.S.A., Inc.
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Recent recall archives
Browse recent months with enough recall history for useful comparison.
October 2026111 records · 4 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