Medicine, medical device and cosmetics recalls in United States
Recalls of medicines, medical devices, supplements, cosmetics and personal care products published in United States, newest first.
1,518 recalls, newest first · Checked 12 minutes ago
United StatesAbbott Diagnostics Scarborough, Inc. recalls Product Name: ID NOW" Influenza A & B 2 Model/Catalog Number: 427-000 Software Version…
It was confirmed that the impacted lot has a higher occurrence of invalid rates when compared to the product Instructions for Use.Hologic, Inc. recalls Brand Name: Aptima HPV Assay Product Name: Aptima HPV Assay Model/Catalog Number: 303585…
Due to product exhibiting potential to generate either invalid or false negative results.Stryker Medical Division of Stryker Corporation recalls Cub Pediatric Crib
Cribs sold in the USA are missing two access door warning labels.LeMaitre Vascular, Inc. recalls Artegraft Vascular Graft
Labeling mix-up resulting in the incorrect lot outer packaging of product.ConvaTec, Inc recalls Convatec and 2 more products
Drainable large pouch may leak due to manufacturing issue.Diagnostica Stago, Inc. recalls Brand Name: STA Liatest D-Di Product Name: STA Liatest D-Di Model/Catalog Number: REF…
After receiving customer complaints, investigations confirmed the presence of a positive bias in D-Dimer measurements throughout the entire analytical range.GE Medical Systems, LLC recalls Centricity Universal Viewer Software Versions 7.0 through 7.0 Sp2.0.1 and 2 more products
There is a potential cybersecurity vulnerability affecting certain versions of Centricity Universal Viewer.Elekta, Inc. recalls Brand Name: Leksell Gamma Knife Product Description: Leksell Gamma Knife¿ Perfexion…
Due to adapter not being properly aligned or locked in place.Howmedica Osteonics Corp. recalls MICS3 Angled Sagittal Saw Attachment
A potential issue was identified with the torque strength on the external screws of the MICS3 Angled Sagittal Saw Attachment.Datascope Corp. recalls Battery Charging Station
The Battery Charging Station is an optional dual-bay charger used to charge the Cardiosave IABP Lithium- Ion batteries when they are not being used to operate the IABP.Somerset Therapeutics LLC recalls Dexamethasone Sodium Phosphate Injection
Failed Impurities/Degradation Specifications - OOS impurities result observed during long term stability testing at product expiry (24 months) were above specs for…Cardinal Health 200, LLC recalls Webcol Alcohol Prep pad
Non-Sterility: microbial contamination identified as Paenibacillus phoenicisAnnora Pharma Private Limited recalls Pitavastatin Tablets
Presence of foreign tablets/capsules: one Pitavastatin tablet 1mg found in bottle of Pitavastatin tablets 2mgStrides Pharma Inc recalls Children's Ibuprofen Oral Suspension
Presence of foreign substance: the firm received complaints for a gel-like mass and black particles in the product.Apotex Corp. recalls Brimonidine Tartrate/Timolol Maleate Ophthalmic Solution 0.2%/0.5%*
Lack of Assurance of SterilityBoston Scientific Corporation recalls EndoVive Safety PEG Kit
Recall of kits which utilized ChloraPrep Triple Swabsticks from BD.Lutronic Corporation recalls CLARITY II Laser System
Reports of devices sparking/popping and potentially burning patients.Medline Industries, LP recalls Medline Medcrest Surgical Gowns: MDTGXC4J5XL DBQ-GOWN and 1 more products
Fabric may experience premature delamination when using included laundering instructions.Ion Beam Applications S.A. recalls IBA Proton Therapy System
It was identified that eh Universal Beam Triggering Interface (UBTI) is disabled in the Therapy Safety System (TSS) configuration.Becton Dickinson & Company recalls 10mL Non-Sterile BD Luer-Lok Tip Syringe Only. Catalog Number: 301029. 850 bulk…
During the bulk packaging process, some Luer Slip syringes were incorrectly included in a batch designated for Luer Lok syringes.Altruan GmbH recalls Wondfo Streptococcal A At-Home Self-Test. At-home test for group A beta-hemolytic… and 2 more products
Product not cleared by the FDA.Covidien LLC recalls HealthCast "Vital Sync" Remote Patient Monitoring System which consists of: Product…
Due to complaints and investigations stating that alarms from the primary patient bedside monitor was not alarming/being transmitted and received on the remote patient…KOB GmbH recalls MEDLINE UNNA-Z STRETCH ZINC PASTE BANDAGE
Due to labeling error.A little guidance
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