🏥 Medical Devices 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).
All Recalls
95,083 total recalls in our database
Fem IM Nail 16mmdx44cm, Sterile, Rod, fixation, intramedullary and accessories- Specific Knee, Hip and Nail Implants
Zimmer Biomet
🏥 Medical Devices 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.
🏥 Medical Devices 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).
🏥 Medical Devices 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).
🏥 Medical Devices Class I - Dangerous
Potential for an incomplete seal on the inner package, which may result in premature degradation of the suture material.
🏥 Medical Devices 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).
Fem IM Nail 16mmdx42cm, Sterile, Rod, fixation, intramedullary and accessories- Specific Knee, Hip and Nail Implants
Zimmer Biomet
🏥 Medical Devices 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.
🏥 Medical Devices 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).
🏥 Medical Devices Class I - Dangerous
Decrease reactivity of R 1 component.
VITEK¿ 2 Gram Negative Susceptibility card (AST-N355), IVD, REF 421351, 20 cards per carton.
Biomerieux
🏥 Medical Devices 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).
GE Healthcare Discovery Ml DR X-ray system
GE Healthcare
🏥 Medical Devices 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.
🏥 Medical Devices 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).
GE Healthcare Optima CT540 X-ray system
GE Healthcare
🏥 Medical Devices 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.
🏥 Medical Devices 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).
🏥 Medical Devices 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).
🏥 Medical Devices 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).
🏥 Medical Devices 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).
Arrow International is recalling the affected product because the packaging may not be completely sealed, which may compromise sterility.
🏥 Medical Devices 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).
🏥 Medical Devices Class I - Dangerous
Arrow International is recalling the affected product because the packaging may not be completely sealed, which may compromise sterility.