Class I - Dangerous
Zimmer Biomet is initiating a field action for sterile-packaged implants packaged in a single package configuration due to packaging design verification test failures.
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Other Medical Devices
🏥 Medical Devices • 15,809 recalls
Class I - Dangerous
reprocessing instructions do not provide sufficient detailed information for the cleaning, disinfection, and sterilization of these products
GE Healthcare lnnova IGS 540 ACT X-ray system
GE Healthcare
Class I - Dangerous
It was discovered that an issue has been identified that can result in a scan starting before the prescribed delay has completed.
GE Healthcare BrightSpeed X-ray system
GE Healthcare
Class I - Dangerous
It was discovered that an issue has been identified that can result in a scan starting before the prescribed delay has completed.
Class I - Dangerous
reprocessing instructions do not provide sufficient detailed information for the cleaning, disinfection, and sterilization of these products
Class I - Dangerous
Zimmer Biomet is initiating a field action for sterile-packaged implants packaged in a single package configuration due to packaging design verification test failures.
Por fullct fem st 18x200mm, Sterile,
Zimmer Biomet
Class I - Dangerous
Zimmer Biomet Inc. initiated a field action on 02/28/2017 for sterile-packaged implants packaged in two different package configurations due to packaging design verification test failures.
Zimmer Biomet is initiating a field action for sterile-packaged implants packaged in a single package configuration due to packaging design verification test failures.
Cook Inc. is initiating a voluntary recall of the OptiLite Multi-Use Holmium Laser Fibers because it has been identified that the reprocessing instructions do not provide sufficiently detailed information for the cleaning, disinfection, and sterilization of these products.
Class I - Dangerous
Product size listed on the labeling is incorrect.
Philips DuraDiagnost X-ray systems: DuraDiagnost (R1.0, Product Number 712210) DuraDiagnost (R2.0, Product Number 712211) DuraDiagnost (R3.0, Product Number 712211)
Philips Electronics North America
Class I - Dangerous
Tube arm assembly could fall down due to cracked welding joints
Class I - Dangerous
Potential for an incomplete seal on the inner package, which may result in premature degradation of the suture material.
VITEK 2 Anaerobic and Corynebacteria identification card (ANC), REF 21347, 20 cards per carton.
Biomerieux
Class I - Dangerous
The integrity of the product container may be compromised thereby exposing product to moisture which could lead to antibiotic degradation (loss of potency).
Class I - Dangerous
Potential for an incomplete seal on the inner package, which may result in premature degradation of the suture material.
Class I - Dangerous
Potential for an incomplete seal on the inner package, which may result in premature degradation of the suture material.
GE Healthcare Discovery NM/CT 570c X-ray system
GE Healthcare
Class I - Dangerous
It was discovered that an issue has been identified that can result in a scan starting before the prescribed delay has completed.
USPACK-SUTURE KIT; Item Number: US1672
Medtronic
Class I - Dangerous
Potential for an incomplete seal on the inner package, which may result in premature degradation of the suture material.
Class I - Dangerous
It was discovered that an issue has been identified that can result in a scan starting before the prescribed delay has completed.
Class I - Dangerous
Potential for an incomplete seal on the inner package, which may result in premature degradation of the suture material.
GE Healthcare Discovery Ml DR X-ray system
GE Healthcare
Class I - Dangerous
It was discovered that an issue has been identified that can result in a scan starting before the prescribed delay has completed.