Product Recalls in North Dakota
Product recalls affecting North Dakota — including food, drugs, consumer products, medical devices, and vehicles distributed to North Dakota. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,471 recalls have been distributed to North Dakota in the last 12 months.
Showing 14921–14940 of 27,512 recalls
Recalled Item: Bronchovideoscope BF-P160 Recalled by Olympus Corporation of the Americas...
The Issue: The attachment of non-Olympus accessories to the bronchoscope s instrument...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bronchovideoscope BF-3C160 Recalled by Olympus Corporation of the Americas...
The Issue: The attachment of non-Olympus accessories to the bronchoscope s instrument...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips HeartStart Infant/Child SMART Pads Cartridge Recalled by Philips...
The Issue: The recall is being initiated due to incorrect age range labeling (8+ yrs)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ImplantDirect Legacy 3 Implant Recalled by Implant Direct Sybron...
The Issue: Two units in distribution were found to be mislabeled on the vial cap with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Minimed Model 500 Remote Control (MMT-500 Recalled by Medtronic Inc. Due to...
The Issue: There is a potential security vulnerability related to the use of the remote...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Minimed Model 503 Remote Transmitter (MMT-503 Recalled by Medtronic Inc. Due...
The Issue: There is a potential security vulnerability related to the use of the remote...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ysio MAX (model number 10762470) with Tube stand 3D V Recalled by Siemens...
The Issue: In rare cases of high clinical workload, the steel cables inside the lifting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Laparoscopy Instruments Instructions For Use (IFU) for the following:...
The Issue: The Manual cleaning process and the usability of the reprocessing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ysio (model number 10281013 or 10281163) with Tube stand 3D Recalled by...
The Issue: In rare cases of high clinical workload, the steel cables inside the lifting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AXIOM Multix MT (model number 8395415 or 8395399 or 8395381) Recalled by...
The Issue: In rare cases of high clinical workload, the steel cables inside the lifting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Multix Fusion system is a radiographic system: Models: Multix Fusion...
The Issue: Steel cables inside the lifting column of the overhead tube, may rapture...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vanguard 360 Revision Knee System 63x 10mm Universal Tibial Block Augment...
The Issue: The implant only has one bolt in the sterile package but it should have had two.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Palcam Agar Base Recalled by Acumedia Manufacturers, Inc. Due to Expiration...
The Issue: Expiration date on the label is incorrect. Correct expiration date was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vanguard 360 Revision Knee System 75x 5mm Universal Tibial Block Augment...
The Issue: The implant only has one bolt in the sterile package but it should have had two.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kerlix Gauze Roll Recalled by COVIDIEN LLC Due to Potential for product...
The Issue: Potential for product sterility breach due to a compromised or pinched seal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kerlix AMD Antimicrobial Bandage Roll Recalled by COVIDIEN LLC Due to...
The Issue: Potential for product sterility breach due to a compromised or pinched seal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kerlix Bandage Roll Recalled by COVIDIEN LLC Due to Potential for product...
The Issue: Potential for product sterility breach due to a compromised or pinched seal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kerlix Bandage Roll Recalled by COVIDIEN LLC Due to Potential for product...
The Issue: Potential for product sterility breach due to a compromised or pinched seal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dermacea Gauze Fluff Roll Recalled by COVIDIEN LLC Due to Potential for...
The Issue: Potential for product sterility breach due to a compromised or pinched seal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dermacea Gauze Fluff Roll Recalled by COVIDIEN LLC Due to Potential for...
The Issue: Potential for product sterility breach due to a compromised or pinched seal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.