Medicine, medical device and cosmetics recalls
Recalls of medicines, medical devices, supplements, cosmetics and personal care products.
2,324 recalls, newest first · Checked 12 minutes ago
United StatesThe Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories recalls Major ChlorproMAZINE Hydrochloride Tablets and 4 more products
CGMP Deviations: Presence of N-Nitroso Desmethyl Chlorpromazine above the recommended intake limitAvKARE recalls Norgestimate and Ethinyl Estradiol Tablets
Failed Content Uniformity SpecificationsGenoGenix LLC recalls Alpha Lipoic Acid for Injection and 56 more products
Lack of Assurance of Sterility Microbial Contamination of Sterile Products: elevated endotoxin levels
CanadaDual Mobility Vivacit-E® Vitamin E Bearing
Zimmer Biomet is conducting a medical device recall for one (1) lot of the Dual Mobility Vivacit-E® bearing due to a commingle.Catalyft™ PL Expandable Interbody System, Interbody Cage
This notification is to inform customers of the potential for loss of lordosis and ensure that they are aware of updates that Medtronic is making to the surgical…
Culture Kizos inc./Kizos Culture inc. recalls Coterie Double-Infused Fruity Pebbles Blunt due to microbial contamination
The affected products may contain mould.Atlantiscan: Broken Vials
The vial is broken in affected lot.ITOVEBI (inavolisib) and the Risk of Life-Threatening Ketoacidosis
Two cases of life-threatening or fatal ketoacidosis have been reported in diabetic patients treated with ITOVEBI in the post-market setting.
United KingdomAngel Cosmetics Clairmen Lightening Program for Men safety warning
The product presents a serious chemical risk as it has been found to contain hydroquinone, which is a skin sensitiser and may cause allergic contact dermatitis.LOGIQ P10
GE Healthcare has become aware of an issue on certain LOGIQ P9 and LOGIQ P10 series ultrasound systems with system software version R4.5.7.Low Prof Lckng Screw F/Im Nail, Sterile
The affected product lots are being recalled because, although the etched length on the screw is correct, the length marked on the external packaging is incorrect.Magseed Pro Magnetic Marker System
During residual and particulates testing it was discovered that cotton fibers were present on the markers.Lisinopril HCT 20/25mg: Out-of-specification test results
Affected lots were recalled following assay stability out-of-specification test results.W L Gore & Associates, Inc. recalls GORE ACUSEAL Vascular Graft
Reports of vascular graft delamination, which may lead to reduced access flow; cannulation difficulties; bleeding or bruising; and harms related to reintervention…Bard Peripheral Vascular Inc recalls Venclose digiRF Generators
Software version 3.35 of the Venclose digiRF Generator incorporates a catheter verification feature specifically designed to detect internal wiring anomalies in…S.I.N. Implant System Ltda recalls IMPLANT EPIKUT PLUS MT16 3
Dental implants were imported under temperature and storage conditions that do not comply with the instructions for use and product labeling so there may be packaging…Beckman Coulter Inc. recalls DxC 500 AU Module w/ISE
On a clinical analyzer, when ordering a Clinical Chemistry (CC) combination test simultaneously with an Immunoassay (IA) test, if the IA test is processed between the…bioMerieux, Inc. recalls VITEK¿ 2 Gram-negative AST Test Kits
Potential for false resistant results for Colistin (cs02n) with multi-drug-resistant Pseudomonas aeruginosa and Acinetobacter baumannii complex used in specific cardsLeMaitre Vascular, Inc. recalls Artegraft Collagen Vascular Grafts Model Numbers:
The bovine carotid arteries used to produce the impacted grafts from affected lots were sourced using raw material from a supplier that had not been reviewed and…Medline Industries, LP recalls Medline Kits: 1) VALVE PACK-LF
The kits contain certain lots of cannula products where the catheter may not retain its shape.Change Healthcare Canada Company recalls Change Healthcare Radiology Solutions software version 14.2.2
Due to software issue, radiology reports may not be fully displayed when viewing.Howmedica Osteonics Corp. recalls 1. EXETER V40 STEM 44MM NO 2
a potential product mix where the package labeled as Catalog Number 0580-1-442, lot A00976, may contain Catalog Number 0580-1-352, lot G8754849, and vice versa.Medline Industries, LP recalls Sterile Medline Convenience Kits: 1) MAJOR PACK L-F and 1 more products
Convenience kits labeled as sterile have not gone through the sterilization process.A little guidance
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