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 5 minutes ago
United StatesOtsuka ICU Medical LLC recalls 0.9% Sodium Chloride Injection
Product Mix-up: 0.9% SODIUM CHLORIDE Injection, USP may potentially contain the overwrap with labeling indicating it to be 0.9% SODIUM CHLORIDE Injection, USP but the…Amneal Pharmaceuticals of New York, LLC recalls Exenatide Injection
Defective Delivery System: Possibility of no medication in the prefilled pen.Insight Pharmaceuticals LLC, a Prestige Consumer Healthcare company recalls Clear Eyes Redness Relief and 1 more products
Lack of Assurance of SterilitySterling Pharmaceutical Services LLC recalls AvKare Carboxymethylcellulose Sodium Ophthalmic Solution 0.5% and 8 more products
Lack of Assurance of SterilityMedical Action Industries, Inc. 306 recalls Blood Culture Collection Venipuncture Kit 20/Cs
Blood culture convenience kits contain a component subject to a drug recall that due to an an open or incomplete seal on the packaging of the applicator may compromise…Nuclein LLC recalls Brand Name: DASH Rapid PCR Instrument Product Name: DASH Rapid PCR Instrument…
Due to a software issueICU Medical, Inc. recalls CADD Yellow Medication Cassette Reservoir with NRFit connector US Product Codes…
Reservoirs may exhibit medication leakage at the joint between luer connector and tubing.restor3d Inc. recalls Kinos Axiom Total Ankle System with Axiom PSR
Ankle implantation systems were packaged with incorrect patient-specific cutting guides, which may result in: delayed surgery, the need to use standard instrumentation…BD Switzerland Sarl recalls BD Alaris Pump Infusion Sets 10561554* 10885403232565 50885403232563 BD Alaris Pump…
Due to discrepancies in specific attributes in the performance data for infusion sets, which may lead to inappropriate pump performance.Well Lead Medical Co. LTD recalls SunMed Tracheal Tube
The 6Fr suction catheter could not pass through the samples smoothly.Straumann USA LLC recalls GM Helix Implant
There is a discrepancy between the product identification on the packaging and the dimensions of the implant contained inside.embecta Medical II LLC recalls EWO_02512 and 1 more products
Retrospectively reported: Pen needles labeled 'For Investigational Use Only' were inadvertently distributed as commercially marketed devices.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 are contaminated with Aspergillus penicillioidesBard Access Systems, Inc. recalls Power-Trialysis Short-Term Straight Dialysis Catheter and 1 more products
this is a downstream recall of class I recall RES 98777PTW Freiburg recalls Brand Name: VERIQA
When a bolus is included in a treatment plan and sent for secondary dose calculation, the software accounts for it but does not display this clearly, which may lead…Noxbox LTD recalls NOxBOXi Nitric Oxide Delivery System.
Potential for oxygen tubing leaks due to failure of the tubing or tubing connection, which may lead to oxygen desaturation.Medline Industries, LP recalls Convenience kits ANESTHESIA PAIN PK LEAGUE DYNJ67925A and 3 more products
Kits may exhibit open seals in sterile pouch packaging.Boston Scientific Corporation recalls Boston Scientific Corporation StoneSmart Connect Console Contents:
A subset of power adapters used with the connect console may exhibit higher-than-expected resistance in the electrical grounding path.Maquet Cardiopulmonary Gmbh recalls Percutaneous Insertion Kit and 2 more products
The packaging may not consistently maintain sterile barrier integrity.Wilson-Cook Medical Inc. recalls Brand Name: HEMOSPRAY ENDOSCOPIC HEMOSTAT Product Name: HEMOSPRAY ENDOSCOPIC HEMOSTAT…
Due to issue with endoscope adherence and inability to spray powder.Bayer Medical Care, Inc. recalls MEDRAD¿ Stellant FLEX Syringe Kit used with Stellant FLEX CT Injection System
Some devices may not have been properly sterilized due to a manufacturing sterilization issue.Pi Cardia LTD recalls Pi-Cardia Inc. ShortCut REF: Z-A-20.003-US
Transfemoral catheter, positing arm may detached due to weld issue.Mirion Technologies (Capintec), Inc. recalls Captus 4000e Thyroid Uptake System
Potential for failure of the tension bolt which would allow the spring arm to unexpectedly fall to its lowest position, which is approximately 25 inches (63.5 cm) from…A little guidance
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