DrugOct 6, 2021
Johnson & Johnson Consumer Neutrogena Beach Defense water+sun protection sunscreen spray recall — FDA D-0841-2021
cGMP Deviations
Class IIFDA: OngoingJohnson & Johnson Consumer, Inc.
Latest records
Latest recalls — page 818
The newest recall records with useful source details are listed here.
DrugOct 6, 2021
Washington Homeopathic Products Humulus 6X, 15X, Sucrose/Lactose Pills, 6X Packaged as a) recall — FDA D-0866-2021
Out-of-specification test results obtained for identification testing based on HPTLC analysis.
Class IIFDA: TerminatedWashington Homeopathic Products, Inc.
DrugOct 6, 2021
Washington Homeopathic Products ZTE-1034 Formula Antimicrobial Bowel recall — FDA D-0885-2021
Out-of-specification test results obtained for identification testing based on HPTLC analysis.
Class IIFDA: TerminatedWashington Homeopathic Products, Inc.
DrugOct 6, 2021
Johnson & Johnson Consumer Neutrogena COOLDRY SPORT sunscreen spray BROAD SPECTRUM SPF 50 recall — FDA D-0834-2021
cGMP Deviations
Class IIFDA: OngoingJohnson & Johnson Consumer, Inc.
DrugOct 6, 2021
Washington Homeopathic Products ZTE-105 Formula Gentle Detoxing recall — FDA D-0858-2021
Out-of-specification test results obtained for identification testing based on HPTLC analysis.
Class IIFDA: TerminatedWashington Homeopathic Products, Inc.
DrugOct 6, 2021
Johnson & Johnson Consumer Neutrogena Ultra Sheer body mist sunscreen BROAD SPECTRUM SPF 30 recall — FDA D-0836-2021
cGMP Deviations
Class IIFDA: OngoingJohnson & Johnson Consumer, Inc.
DrugOct 6, 2021
Johnson & Johnson Consumer Neutrogena Beach Defense water+sun protection sunscreen spray recall — FDA D-0849-2021
cGMP Deviations
Class IIFDA: OngoingJohnson & Johnson Consumer, Inc.
DrugOct 6, 2021
Washington Homeopathic Products Aconitum nap Fear* Sucrose/Lactose Pills HPUS: 4X, 5X recall — FDA D-0892-2021
Out-of-specification test results obtained for identification testing based on HPTLC analysis.
Class IIFDA: TerminatedWashington Homeopathic Products, Inc.
DrugOct 6, 2021
Johnson & Johnson Consumer Neutrogena Beach Defense water + sun protection sunscreen spray recall — FDA D-0833-2021
cGMP Deviations
Class IIFDA: OngoingJohnson & Johnson Consumer, Inc.
DrugOct 6, 2021
Johnson & Johnson Consumer Neutrogena Invisible Daily defense body spray sunscreen BROAD recall — FDA D-0843-2021
cGMP Deviations
Class IIFDA: OngoingJohnson & Johnson Consumer, Inc.
DrugOct 6, 2021
Washington Homeopathic Products Occular Allergy Blend 87% Alcohol recall — FDA D-0859-2021
Out-of-specification test results obtained for identification testing based on HPTLC analysis.
Class IIFDA: TerminatedWashington Homeopathic Products, Inc.
VehicleOct 1, 2021
Bronco frontal air bag recall — NHTSA campaign 21V770000
Ford Motor Company (Ford) is recalling certain 2021 Bronco vehicles. During passenger air bag deployment, an air bag vent could open prematurely and result in an improper deployment. As…
frontal air bagFord Motor Company
Medical DeviceSep 29, 2021
Ad-Tech TECH ATTACH Cable- Product Usage: Designed for the purpose of connecting these recall — FDA Z-2496-2021
Incorrect version of labels were used.
Class IIFDA: TerminatedAd-Tech Medical Instrument Corporation
Medical DeviceSep 29, 2021
Microbiologics SARS-CoV-2 Process Control (Swab) - Product Usage: intended for use as an recall — FDA Z-2487-2021
The product indicated is contaminated with a plasmid DNA that contains the target SARS-CoV-2 sequences.
Class IIFDA: TerminatedMicrobiologics Inc.
Medical DeviceSep 29, 2021
Greiner Bio-One VACUETTE TUBE 2 ml 9NC Coagulation sodium citrate 3.2% 13x75 blue cap-white recall — FDA Z-2507-2021
Complaint of tubes clotting due to variation of anticoagulant and/or tubes have low vacuum.
Class IIFDA: TerminatedGreiner Bio-One North America, Inc.
Medical DeviceSep 29, 2021
Sight OLO-E1/U1 Software and Operators Manual Software v2.56.1 Catalog #: 1 OLO-U1 Catalog recall — FDA Z-2517-2021
Discrepancy in labeling between the adult CBC reference ranges presented in the OLO Operator's Manual and the OLO software
Class IIFDA: TerminatedSIGHT DIAGNOSTICS LTD
Medical DeviceSep 29, 2021
Beckman Coulter Access SARS CoV-2 IgG (1st IS) Assay: Access Immunoassay Systems REAGENT recall — FDA Z-2508-2021
Firm's submission for Emergency Use Authorization (EUA) contained insufficient evidence to be granted EUA Authorization to distribute
Class IIFDA: TerminatedBeckman Coulter Inc.
Medical DeviceSep 29, 2021
Aesculap Implant Systems Univation X System knee implant devices as follows recall — FDA Z-2511-2021
Malfunction- loosening of the implant resulting in a potential revision surgery
Class IIFDA: TerminatedAesculap Implant Systems LLC
Medical DeviceSep 29, 2021
Aesculap Implant Systems Univation X System knee implant devices as follows recall — FDA Z-2512-2021
Malfunction- loosening of the implant resulting in a potential revision surgery
Class IIFDA: TerminatedAesculap Implant Systems LLC
Medical DeviceSep 29, 2021
Aesculap Implant Systems Univation X System Tray Sysem knee implant devices as follows: Tray recall — FDA Z-2516-2021
Malfunction- loosening of the implant resulting in a potential revision surgery
Class IIFDA: TerminatedAesculap Implant Systems LLC
Medical DeviceSep 29, 2021
In2bones USA CoLink Bone Graft Harvester, 8mm, Sterile, Disposable, REF G05 S1008 - Product recall — FDA Z-2506-2021
Complaints were received of CoLink Bone Graft Harvesters breaking at the outer tube weld site.
Class IIFDA: TerminatedIn2bones USA, LLC
Medical DeviceSep 29, 2021
Philips Ultrasound EPIQ Diagnostic Ultrasound Systems: Software Versions 5.0, 5.0.1 and recall — FDA Z-2483-2021
Due to a software defect that can intermittently cause the system to lock-up which exiting Review Mode while performing an exam.
Class IIFDA: CompletedPhilips Ultrasound Inc.
Medical DeviceSep 29, 2021
Mac Medical Supply Co Ultrasound Gel labeled under the following brand names: MediChoice recall — FDA Z-2469-2021
Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may contain bacterial contamination.
Class IFDA: OngoingMac Medical Supply Co Inc.
Medical DeviceSep 29, 2021
Philips Ultrasound Affiniti Diagnostic Ultrasound Systems: Software Versions 5.0, 5.0.1 and recall — FDA Z-2484-2021
Due to a software defect that can intermittently cause the system to lock-up which exiting Review Mode while performing an exam.
Class IIFDA: CompletedPhilips Ultrasound 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