Medicine, medical device and cosmetics recalls
Recalls of medicines, medical devices, supplements, cosmetics and personal care products.
222 recalls match · Clear filters · Checked 2 minutes ago
United StatesMedline Industries, LP recalls Medline Convenience Kit: OPEN HEART A PACK
The kits contain a Retrograde Coronary Sinus Perfusion (RCSP) cannulae that has the potential for a sterile barrier breach.Medline Industries, LP recalls Medline Convenience Kits: 1) KIT ANESTHESIA L&D A- LINE SET and 6 more products
The kits contain certain lots of sterile applicators which may contain fungal contamination that may occur under certain environmental conditions, allowing the growth…AVID Medical, Inc. recalls Haylard 18G SINGLE SHOT EPI TRAY and 3 more products
Potential for product quality and sterility issues regarding kits containing Sodium Chloride ampules subject to recall by Spectra Medical.Pfizer recalls Dopamine HCl Inj.
Lack of Assurance of Sterility
United KingdomBaylis & Harding Oud, Cedar & Amber 1L Hand Wash Refill recall
The product presents a microbiological risk as testing identified the presence of Pluralibacter gergoviae.AVID Medical, Inc. recalls Halyard IV Start Kit Non-Sterile REF: KRIV26-02
Convenience kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which lacks sterility assurance due to to wrinkles in the paper lidding which may…Medical Action Industries, Inc. 306 recalls Kit: Epidural/Pain TQC 20/Cs and 1 more products
Kits containing Sodium Chloride ampules subject to another recall are recalled due to potentially compromised sterility.Atrium Medical Corporation recalls Getinge PVC Thoracic Catheter and 2 more products
An Out of Specification result (OOS) related to bacterial endotoxin testing in a single lot of catheters.C.R. Bard Inc recalls Products that contain the Pericare Wipes: Bardex Lubricath Foley Catheter Tray REF… and 5 more products
Due to complaints received indicating presence of contamination on the surface of pericare wipes provided with various Foley and Intermittent Catheter Trays.American Regent, Inc. recalls Epinephrine Injection
Presence of Particulate Matter and Lack of Assurance of Sterility.
AustraliaColoured contact lenses designed for cosplay and makeup applications recall
The packaging solution for these contact lenses may be contaminated with Burkholderia cepacia complex bacteria.Medline Industries, LP recalls Medline Convenience Kits containing BD ChloraPrep Clear and 12 more products
Convenience kits contain BD ChloraPrep Clear - 1mL Applicators from specific lots that were recalled by the manufacturer because they may have an open or incomplete…Cardinal Health 200, LLC recalls Presource Packs Containing CliniClean Pericare Wipes within BD Urinary Catheter Trays… and 11 more products
The Urinary Catheter Trays contain CliniClean Pericare Wipes which may potentially be contaminated with a lubricant used during the manufacturing process.Medline Industries, LP recalls Medline Convenience Kits: 1) DRAWER 9 CRICOTHYROTOMY KIT and 15 more products
The kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which have a potential breach of sterility in the packaging, due to wrinkles in the paper…Sage Products, LLC recalls 2% Chlorhexidine Gluconate* Cloth
Cross Contamination with Other ProductsLexia LLC recalls Broadway Joe's Pain Cream and 1 more products
CGMP Deviations: Potential contamination of raw materialOptimal Balance Pharmacy recalls Glutathione 200 mg/mL
Microbial Contamination of Sterile Products - out of specifications results were obtained for bacterial endotoxin.
CanadaLEO+ Intracranial Self Expandable Stent And Delivery System
As a precautionary measure, Balt Extrusion is voluntarily recalling specific ANRYV connector lots after routine quality control identified non-conforming bacterial…Quantum PureFlow Standard Heat Exchanger High Flow
Blood-to-glycol leakage was identified in the heat exchanger during the procedure.Medline Industries, LP recalls Medline convenience kits labeled as: 1) FEMORAL PACK and 10 more products
Kits contain a potentially contaminated component which were recalled by the manufacturerChurch & Dwight Co., Inc. recalls Zicam
CGMP Deviations; FDA inspection of the contract manufacturer noted out of limit results for microbiological testingBIOFIRE® Joint Infection Panel – 30 Pack
Beginning April 5, 2026, elevated rates of KPC unexpected positives were observed in reagent final QC testing of the BIOFIRE® FILMARRAY® Pneumonia Panel, BIOFIRE®…Arrowhead DE LLC recalls Arrow-LOK Implant
Implant did not undergo required gamma radiation dose audit.A little guidance
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