Preformance Post Dental implants
Biomet 3i
🏥 Medical Devices Class I - Dangerous
Pouches may not have been sealed during packing.
All Recalls
95,094 total recalls in our database
🏥 Medical Devices Class I - Dangerous
Pouches may not have been sealed during packing.
🏥 Medical Devices Class I - Dangerous
Internal investigation found the certain lots of MRSA kits have the potential for performance issues at lower positive sample concentrations.
Hospira has become aware of customers using the incorrect size Receptal liners with their Receptal canisters, e.g., 1.5 L liner, 2L liner or 3L liner with a 1L canister. It is possible that if an incorrectly sized liner is used with a different size canister the lid may not fit and the vacuum/suction will not be sufficient and/or consistent.
🏥 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.
🏥 Medical Devices Class I - Dangerous
Potential for compromise of the package resulting in a breach of the sterile barrier
🏥 Medical Devices Class I - Dangerous
Potential for compromise of the package resulting in a breach of the sterile barrier
Convenience Kits, MOHS "OPENING" PROCEDURE 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.
🏥 Medical Devices Class I - Dangerous
Pouches may not have been sealed during packing.
Gingihue Post Dental implants
Biomet 3i
🏥 Medical Devices Class I - Dangerous
Pouches may not have been sealed during packing.
Xario 100 Diagnostic Ultrasound System, TUS-X100; Xario 200 Diagnostic Ultrasound System, TUS-X200.
Toshiba American Medical Systems
🏥 Medical Devices Class I - Dangerous
Toshiba American Medical Systems (TAMS) is recalling the Xario Diagnostics Ultrasound System because it may become hot because of a software error.
🏥 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.
🏥 Medical Devices Class I - Dangerous
DePuy Synthes is voluntarily initiating a recall due to a possibility the fastener on the Titanium Single Vector Distractor Body may become prematurely separated from the Proximal Foot Plate.
Titanium Square Uniscrew 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
Pouches may not have been sealed during packing.
🏥 Medical Devices Class I - Dangerous
Pouches may not have been sealed during packing.
Quickbridge TM Cap Dental implants
Biomet 3i
🏥 Medical Devices Class I - Dangerous
Pouches may not have been sealed during packing.