Medicine, medical device and cosmetics recalls
Recalls of medicines, medical devices, supplements, cosmetics and personal care products.
2,324 recalls, newest first · Checked 5 minutes ago
United StatesPark Avenue Compounding recalls Phenylephrine HCI
CGMP DeviationsSafecor Health, LLC recalls Haloperidol Lactate Injection
Labeling: Not Elsewhere Classified:Incorrect RFID tag labels applied to product by repackaging firm.Blossom Pharmaceuticals recalls Lanashield Skin Barrier and 12 more products
cGMP deviationsGlenmark Pharmaceuticals Inc., USA recalls Bisoprolol Fumarate and Hydrochlorothiazide Tablets
Cross Contamination with Other Products: Testing of reserve samples showed presence of traces of ezetimibe
United KingdomHello by Lionel Richie and Hot by United Colours of Benetton Fragrances sold by Savers Health and Beauty recall
The products present a serious chemical risk as they contain butylphenyl methylpropional (BMHCA/lilial), which is prohibited in cosmetic products.
CanadaNitrous Oxide Chargers: Sold for Inhalation Without Market Authorization (DIN)
The affected products are sold for inhalation without market authorization (DIN) in Canada.Tempus Pro
The user/operator manual references the term 'invasive pressure', which includes intracranial pressure (ICP) and bladder pressure (BDR) as selectable channel labels.Carestation 600 and 700 Series Anesthesia Systems
Unexpected shutdown of Carestation 600 and 700 series anesthesia systems containing certain power management boards when AC mains power is disconnected or AC mains…
JC Green Cannabis Inc. recalls certain Jonny Chronic dried cannabis products due to labelling issue
The labels for the affected products have incorrect cannabinoid values.Yepoda The Cocoa Cloud Body Butter in 2025 Yepoda Advent Calendar recall
Batch SR335 of this product presents a microbiological risk as testing has indicated that it loses efficacy over time, which may lead to the growth of Pseudomonas…Zeus Infinity Empowered (Anesthesia Workstation)
The action is being initiated due as a cybersecurity vulnerability was discovered as part of an internal SW penetration test.Benevision Central Monitoring System (CMS)
Shenzhen Mindray has identified that when the workstation number 115-050935-00 of the Benevision Central Monitoring (CMS) System has a specific hardware configuration…Mucus & Phlegm relief extra strength: may have been exposed to temperatures outside of the recommended storage conditions
Affected lots may have been exposed to temperatures outside of the recommended storage conditions.Sure Hoof: Affected lot is missing some ingredients on the label
Affected lot is missing some ingredients on the label.Zimmer® Air Dermatome and Zimmer® Dermatome AN handpieces
Zimmer Biomet is conducting a phased serial specific medical device recall for the Zimmer® Air Dermatome and Zimmer® Dermatome AN handpieces.PMS-Zolpidem ODT 10mg: Missing tablets in blister packs
Affected lot may be missing tablets in blister packsFlexor® Check-Flo Introducer and Rösch-Uchida Transjugular Liver Access Sets
Cook Medical identified that products supplied in the affected device lots may have been manufactured out of specification.FreeStyle Libre® 3 Plus Sensor Kit
A subset of FreeStyle Libre® 3 plus sensors may provide incorrect low glucose readings.Cardinal Health ChemoPlus™ sleeves and gowns
The product codes and lots listed of Cardinal Health ChemoPlus™ sleeves and gowns were incorrectly labeled with a 5-year expiration date, whereas the product should…Remel, Inc recalls 1. CAMHB W/LHB
Products may contain contamination, which may result in a darker or brown media color.Philips Medical Systems Nederland B.V. recalls Philips Azurion 7M20 systems with FlexArm ceiling-mounted system. Model Number: 722234
The motorized longitudinal movement of the FlexArm stand may be inconsistent (not smooth) and eventually may become unavailable.BioFire Diagnostics, LLC recalls BioFire Respiratory Panel 2.1
Due to unintended movement of pouch chemistry, nucleic acid test may result in elevated risk of false negative results and risk of control failures.Medtronic Sofamor Danek USA Inc recalls Catalyft PL & PL40 Expandable Interbody System labeled as follows with corresponding…
Expandable interbody system cage may loose height or collapse (loss of lordosis), which could result in migration, subsidence and/or neurological injury.A little guidance
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