Medicine, medical device and cosmetics recalls
Recalls of medicines, medical devices, supplements, cosmetics and personal care products.
2,304 recalls, newest first · Checked 18 minutes ago
Beckman Coulter Inc. recalls REF # D23352 and 1 more products
Analyzers contain incorrect algorithms which may affect antimicrobial susceptibility test results, leading to false susceptibility classifications."GE Medical Systems Information Technologies Inc recalls GE Healthcare MAC VU360
Software issue issue with the MAC VU360 v3.0 system.Integrated Medcraft LLC recalls FORWARD Oral Airway Kit and 1 more products
Devices could potentially contain an occluded or partially occluded Guedel Airway tip.Oxos Medical Inc recalls Brand Name: OXOS Medical
Due to a defective circuit board that overheatsSiemens Healthcare Diagnostics, Inc. recalls Atellica CH Urine Albumin REF: 11537225
Processing of urine albumin assay on the CI analyzers may lead to the following issues: Falsely depressed Atellica CH Urea Nitrogen (UN_c) results; Falsely depressed…United Orthopedic Corp. recalls Brand Name: U2 Total Knee System Product Name: PSA Box Trial and 3 more products
Due to an incomplete process of the component screw by a subcontractor which prevents the properly assembling of stem trail.Siemens Healthcare Diagnostics, Inc. recalls Syva Emit tox Serum Tricyclic Antidepressant Calibrator/Controls SMN 10445390 Catalog…
out-of-specification sodium azide concentration in Syva Emit Tox Serum Tricyclic Antidepressant Calibrator/Controls Lot U2.Zydus Pharmaceuticals (USA) Inc recalls Mirabegron Extended-Release Tablets
CGMP: Due to Out of Specification (OOS) result for N-Nitroso Mirabegron impurity.Central Admixture Pharmacy Services Inc recalls Total Parental Nutrition
Incorrect Product FormulationSunny Pharmtech Inc. recalls Cyclophosphamide for Injection and 1 more products
Presence of Particulate Matter; identified as stainless steelAurobindo Pharma USA Inc recalls Dicyclomine Hydrochloride Capsules
shortfill; reports of empty capsules.TEVA-ECTOSONE 0.1% Cream; Affected lot may be missing lot number and expiry date
Affected lot may be missing the lot number and expiry date on the label.Bravo - Capsule Delivery System
Medtronic has identified an increase in complaints involving the Bravo CF capsule delivery device where the capsule fails to attach to the esophagus or detach from the…Fresh Wipes Intimate Unscented Wipes recall
It has been identified that affected batches may be microbiologically contaminated, with the preservative system not performing as required.One lot of New Roots Herbal Probiotic Intensity recalled due to incorrect “No Dairy” claim
New Roots Herbal Inc.HEALON EndoCoat PRO
Johnson & Johnson Surgical Vision, Inc.Beckman Coulter AU Immunochemistry System - AU480 Analyzer
Beckman Coulter has determined that a software defect in AU480 chemistry analyzers using Microsoft® SQL server 2022 express may cause a DB connection error that renders…1788 4K Camera
Stryker Endoscopy has received an increase in complaints for 1788 out of box failures due to bent connection pins.Med-RX Wound Care Kits
Affected lots of BD Chloraprep™ 1 ml applicator (clear) used in CHS Ltd.'s Med-RX wound care kit may exhibit an open/incomplete seal on packaging of the applicator.FilmArray® NGDS Warrior Panel
Testing has identified a potential reduction in sensitivity to the 2026 Bundibugyo outbreak strain which could result in Orthoebolavirus SPP.RELLET Hyaluronic Acid Deep Hydrating Spray recalled due to missing mandatory hazard labelling
The recalled products do not have mandatory hazard labelling as required by the Cosmetic Regulations under the Food and Drugs Act.JAMP Methotrexate 10 mg Tablets: Affected lots may contain oversized tablets.
Affected lots may contain oversized tablets.Medical Action Industries, Inc. 306 recalls Pack Angiography NCMC 3/Cs BANNER
Cardiovascular procedure kits contain manifolds, the subject of another recall, that may have particulate within the fluid path, which has the potential to be…A little guidance
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