Medicine, medical device and cosmetics recalls
Recalls of medicines, medical devices, supplements, cosmetics and personal care products.
2,315 recalls, newest first · Checked 2 minutes ago
Canada
United StatesBioFire Diagnostics, LLC recalls Biofire Spotfire Respiratory/Sore Throat Panel REF: 423485
Respiratory/sore throat panel test may result in false negative results and control failures.Mint Medical GmbH recalls Mint Lesion
If the connection between a mint Lesion workstation and the mint Lesion server is interrupted while performing a read, in rare cases some information may be lost or…Intuitive Surgical, Inc. recalls Intuitive 8 mm SureForm 30 Gray Reloads Reference Numbers: 48230M-05 and 48230M-06
Reloads for curved-tipped stapler may potentially produce an incomplete staple line.Cook Incorporated recalls Centimeter Sizing Catheter RPN N5.0-35-100-P-10S-PIG-CSC-20 GPN G11916 Catheters for use… and 2 more products
Marker bands may be at an increased risk of cracking/breakage.Medical Action Industries, Inc. 306 recalls Medical Action Industries Inc. Pack Cath BHH
Convenience kit contains a syringe in which the rotating adapter may unwind during use, resulting in a loose connection and/or full disconnection between the syringe…Intuitive Surgical, Inc. recalls Brand Name: Da Vinci X and Da Vinci Xi Product Name: da Vinci X
Due to manipulator containing screws with in the arm sub-assembly that my be susceptible to breaking.Orthorebirth Co Ltd recalls BioCera Fibers and 1 more products
Resorbable bone void filler falls outside standard specifications.Erbe Medical, LLC recalls ERBEFLO CleverCap CO2: Hybrid CO2 Tubing/Cap Set for Olympus Scopes & CO2 Sources and 2 more products
Devices providing sterile water/CO2/air to endoscopes were manufactured with a distal irrigation segment connector configuration that may be more susceptible to…Boston Scientific Corporation recalls LUX-DX II and 1 more products
For some patients upgraded from a LUX-Dx M301 device to a new Model M302 or M312, the new ICM device is not collecting PVC Burden data (both M302/M312) or monitoring…BioFire Diagnostics, LLC recalls BioFire Joint Infection
Contamination to in-vitro diagnostic test may result in false positives.Ventec Life Systems, Inc. recalls VOCSN V+Pro package
Respiratory system intended to provide continuous/intermittent ventilator support, may not have been evaluated under all intended high-pressure conditions during…Katalyst Surgical, LLC recalls DEX Ophthalmic Tissue Forceps and 11 more products
Field Safety Corrective Action for IFU in DEX Forceps and Scissors.Spacelabs Healthcare, Inc. recalls Brand Name: Spacelabs Ultraview SL Command Module Product Name: SL Command Module…
Due to a manufacturing issue (i.e.American Contract Systems Inc recalls Convenience kits containing Medline Namic Angiographic Control Syringes with Rotating…
Impacted kits contain syringes recalled by Medline Industries.Physio-Control, Inc. recalls LIFEPAK 15
Some defibrillators serviced between July 2023 through November 2025 were serviced without objective evidence that a Performance Inspection Procedure (PIP) was…Centinel Spine, Inc. recalls Prodisc C SK U.S. IMPLANT EXTRA LARGE 5MM. Model: PDSXL5 Total cervical disc replacement. and 1 more products
Product labeling mix up.DFI Co., Ltd. recalls One Step 10A in vitro diagnostic test and 6 more products
The devices were distributed without required FDA premarket clearance or approval.AVID Medical, Inc. recalls Halyard CARDIAC CATH PACK kit. Model Number: EAMC1000-05 and 9 more products
Potential risk for Medline syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and…Medline Industries, LP recalls Medline Convenience Kits: 1) ANCILLARY PACK-LF and 41 more products
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices.Teva Pharmaceuticals USA, Inc recalls Octreotide Acetate for Injectable Suspension
Lack of Assurance of Sterility: Quality system deficiencies identified during a routine U.S Food and Drug Administration (FDA) inspection at the contract manufacturer.Fresenius Medical Care Holdings, Inc. recalls DELFLEX and 1 more products
Lack of Assurance of Sterility: Potential leaks from perforations in bags.B Braun Medical Inc recalls Lactated Ringer's Injection USP
Presence of Particulate Matter.Breckenridge Pharmaceutical, Inc. recalls Duloxetine Delayed-Release Capsules USP
CGMP Deviations; presence of N-nitroso-duloxetine impurity above the FDA recommended limitA little guidance
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