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 6 minutes ago
United StatesHowmedica Osteonics Corp. recalls AXLE PIN ASSY LARGE ELBOW COBALT CHROME Catalog No. C-M112-2-500 Orthopaedic implant… and 11 more products
Affected devices were manufactured with Ultra High Molecular Weight Polyethylene (UHMWPE) raw material aged in excess of five years.Philips North America recalls Philips Patient Information Center iX REF:866389 and 1 more products
Due to software malfunction, patient information system may freeze and become unresponsive.Abiomed, Inc. recalls Automated Impella Controller and 2 more products
The potential for purge cassette recognition issues due to the failure of the purge flag component of the purge pressure sensor assembly.GE Healthcare recalls Centricity Enterprise Archive V2 and 5 more products
Under certain conditions historical imaging data migrated from a legacy system may become incorrectly associated with a different patient.Happiest Baby, Inc recalls Happiest Baby and 1 more products
Extra small (ES) and Extra-large (XL) infant sleep sacks have not been reviewed for safety and effectiveness by the FDA.Medline 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.ICU Medical, Inc. recalls Plum administration sets and 3 more products
Intravascular administration tubing set drip chambers may have black specks potentially due to the plastic molding process leaving discolored polyvinyl chloride (PVC)…Nova Biomedical Corporation recalls StatStrip Glucose Hospital Meter System. Model No: 63685. Glucose test system. and 4 more products
A software synchronization/timing issue in the barcode scanning and patient data processing component that causes the device to intermittently retain a previously…GE Medical Systems Information Technologies Inc recalls Carescape Central Station CSCS V3 MAS800 Desktop Part Number 5867474-04
Device may not resume patient monitoring for at least 3 minutes following system restart.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.Datex-Ohmeda, Inc. recalls Aisys and 3 more products
Anesthesia Delivery Systems containing certain electronic gas mixer assemblies can automatically transition to Alternate O2 control.Stryker Sustainability Solutions recalls REF:2B5LT Ethicon Endo-Surgery and 5 more products
Reusable access port system may crack or seperate during use.Pfizer recalls Dopamine HCl Inj.
Lack of Assurance of SterilitySun Pharmaceutical Industries Inc recalls Nystatin Cream
Failed Stability SpecificationsInventia Healthcare Limited recalls Chlorthalidone Tablets
Failed Dissolution SpecificationsSun Pharma /Taro recalls Lidocaine Ointment USP
Failed Content Uniformity Specifications.Vitruvias Therapeutics Inc recalls Thyroid Tablets
Superpotent DrugSafecor Health, LLC recalls Fluphenazine HCl Elixir and 5 more products
Failed Stability Specifications
Global Mix Inc. Recalls Niwali Tejocote Capsules and Niwali Tejocote Pieces Because of Possible Health Risk
Products contain yellow oleander (Thevetia peruviana).
Par Health Issues Voluntary Nationwide Recall of Two Lots of Dexmedetomidine HCl in 0.9% Sodium Chloride Injection Due to the Presence of Particulate Matter
Presence of particulate matter identified as cellulose or stopper material
Otsuka ICU Medical LLC Issues Voluntary Nationwide Recall of 0.9% Sodium Chloride Injection, USP Due To a Product Mix-up with 10 mEq Potassium Chloride Injection
Product mix-up where 0.9% Sodium Chloride Injection, USP overwrap may contain 10 mEq Potassium Chloride InjectionGiven Imaging Ltd. recalls Bravo CF capsule delivery device
Capsule may fail to attach to the esophagus or detach from the delivery device.A little guidance
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