Medicine, medical device and cosmetics recalls
Recalls of medicines, medical devices, supplements, cosmetics and personal care products.
2,315 recalls, newest first · Checked 1 minute ago
United StatesIntuitive Surgical, Inc. recalls Brand Name: da Vinci S and 1 more products
Due to increased in complaints regarding frayed or broken pitch cables on reusable surgical instrumentsGE Healthcare LLC recalls SIGNA Premier systems
Whole-Body MR scanners used to produce images of the inside of the human body to aid diagnosis of disease may have been manufactured/serviced with ferrous (steel)…Medline Industries, LP recalls Airway Exam Kit and 6 more products
Kits contain recalled Olympus biopsy valves.Alembic Pharmaceuticals, Inc. recalls Bromfenac Ophthalmic Solution 0.07%
Failed Impurities/Degradation Specifications: out of specification at the time of testing i.e.K.C. Pharmaceuticals, Inc recalls Sterile EYE DROPS AC and 7 more products
Lack of Assurance of SterilityAmneal Pharmaceuticals, LLC recalls Magnesium Sulfate in Water for Injection
Product mix up: a foil pouch labeled "Magnesium Sulfate in Water for Injection, 4 g/100 mL" actually contained an IV bag of Tranexamic Acid instead.Amneal Pharmaceuticals, LLC recalls traMADol Hydrochloride Tablets
Failed Impurities/Degradation Specifications: N-nitroso-desmethyl-tramadol impurity (NDSRI) was found out of the specification at 24-month stability interval during…Appco Pharma LLC recalls Prazosin Hydrochloride Capsules and 2 more products
cGMP deviation: detection of Nitrosamine Drug Substance-Related Impurities, N-nitroso-prazosin impurity C (NNP) above acceptable limits.
CanadaAved products recall: No market authorization
Products sold without market authorization (DIN) in Canada due to third-party branding.Olympus Connecting Tubes
Olympus identified through complaint review that version 2 connecting tubes may fail prematurely, with lock levers detaching or breaking earlier than expected.AneurysmFlow
Philips has determined that the mafa ratio does not provide reliable prognostic information regarding aneurysm occlusion following flow diverter stent treatment.Edwards EVOQUE Tricuspid Delivery System
Edwards Lifesciences is notifying customers of a voluntary recall (correction) involving a labeling update for the Edwards EVOQUE Tricuspid Valve Replacement System.Dimension® Creatinine (CRE2)
Siemens Healthineers has confirmed, through investigation of customer complaints, a potential for imprecision in Dimension® Creatinine (CRE2) quality control (QC) and…Medline Convenience Kits containing Namic RA Syringes
Kits containing Namic Angiographic Rotating Adaptor (RA) Control Syringes (Namic RA Syringes) have been recalled by Medline due to a potential risk of the syringe…Health First Vitamin E capsule; Undeclared active ingredient
Affected lots contain undeclared active ingredient.Kiwi® Vacuum Assisted Delivery System
The device may break at the Traction Force Indicator (TFI) joint during use when traction is applied at approximately a 45-degree angle.DermaHealer UVB Light Therapy Lamps
DermaHealer UVB light therapy devices were distributed to customers in Canada without a Canadian Medical Device Licence (MDL) as required under the Medical Devices…Flamingo Funnel™
Packaging defect: A non-gamma-compatible drape degraded under heat, causing pinholes and possible loss of sterility.Jamieson Laboratories products recall; Tamper-evident seals defective
Tamper-evident seals may be defective in the affected lot(s).Ultraview SLâ„¢ Command Module
It was discovered during production testing that the cardiac output function of the multiparameter module model 91496 was intermittently yielding bad or irregular curves.B. Braun Hemodialysis Blood Tubing Set
The potential for the accumulation of small air bubbles in the arterial line due to adherence of blood gases to the tubing under negative pressure.Medline Industries, LP recalls Puracol and Puracol Plus Collagen Wound Dressings: MSC8522 DRESSING
Elevated endotoxin levels identified in affected lots.Beckman Coulter, Inc. recalls MicroScan Neg MIC 56 REF C42464 UDI-DI code: 15099590731212 MicroScan panels are…
Due to the likely presence of contamination in well(s).A little guidance
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