🏥 Medical Devices Class I - Dangerous
Pouches may not have been sealed during packing.
All Recalls
95,094 total recalls in our database
IOL Distal Extension Dental implants
Biomet 3i
🏥 Medical Devices Class I - Dangerous
Pouches may not have been sealed during packing.
🏥 Medical Devices Class I - Dangerous
Pouches may not have been sealed during packing.
Baxter is issuing a safety alert in response to postmarketing reports received for the VASC U-GUARD Peripheral Vascular Patch. Baxter has received reports for intraoperative or postoperative bleeding episodes, which required additional clinical intervention. One report involved a case with a fatal outcome. UPDATE 9/1/2016 Baxter issued a notice retrieving 6 lots of VASCU-GUARD due to the increased postmarketing reports related to intraoperative and postoperative bleeding.
🏥 Medical Devices Class I - Dangerous
Wire which deploys the loop may be come detached at the handle causing the device to be inoperable
🏥 Medical Devices Class I - Dangerous
Pouches may not have been sealed during packing.
Temporary Hexed Cylinder Dental implants
Biomet 3i
🏥 Medical Devices Class I - Dangerous
Pouches may not have been sealed during packing.
🏥 Medical Devices Class I - Dangerous
Pouches may not have been sealed during packing.
Gold Slotted Screw Dental implants
Biomet 3i
🏥 Medical Devices Class I - Dangerous
Pouches may not have been sealed during packing.
🏥 Medical Devices Class I - Dangerous
Potential for compromise of the package resulting in a breach of the sterile barrier
🏥 Medical Devices Class I - Dangerous
Wire which deploys the loop may be come detached at the handle causing the device to be inoperable
🏥 Medical Devices Class I - Dangerous
Pouches may not have been sealed during packing.
🏥 Medical Devices Class I - Dangerous
Masks in this lot, labelled and sold as 62702 vented Quattro Air FFM size Medium actually contain a non-vented (NV) Quattro Air FFM Large mask.
🏥 Medical Devices Class I - Dangerous
Pouches may not have been sealed during packing.
🏥 Medical Devices Class I - Dangerous
Potential for compromise of the package resulting in a breach of the sterile barrier
🏥 Medical Devices Class I - Dangerous
Mindray has identified a potential leakage issue with the CO2 Module's Dryline II Water Trap used with the Passport Series Patient Monitor.
🏥 Medical Devices Class I - Dangerous
Potential for compromise of the package resulting in a breach of the sterile barrier
MultiQuant MD software where under certain conditions a user can be presented with incorrect quantitative results when using the Sum Multiple Ions feature.
Conical Abutment Dental implants
Biomet 3i
🏥 Medical Devices Class I - Dangerous
Pouches may not have been sealed during packing.
PEDIATRIC KIDNEY BIOPSY TRAY
Avid Medical
🏥 Medical Devices Class I - Dangerous
Avid Medical Inc. states a latex-containing Telfa" Non-adherent Dressing 4"x3" (10.2cm x 7.6 em) was included in a limited number of convenience kits (custom procedure trays) that were not labeled as containing latex.