Product Recalls in New Mexico
Product recalls affecting New Mexico — including food, drugs, consumer products, medical devices, and vehicles distributed to New Mexico. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,862 recalls have been distributed to New Mexico in the last 12 months.
Showing 24161–24180 of 27,850 recalls
Recalled Item: K-Lite Knee 2 Stays with Visco Recalled by Breg Inc Due to Breg is recalling...
The Issue: Breg is recalling the Economy Elastic Knee Sleeve Open and K-Lite Knee 2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Economy Elastic Knee Sleeve Open Recalled by Breg Inc Due to Breg is...
The Issue: Breg is recalling the Economy Elastic Knee Sleeve Open and K-Lite Knee 2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pressure Monitoring Tubing Recalled by Merit Medical Systems, Inc. Due to...
The Issue: The products are labeled as sterile but were not sterilized.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cobas c8000 Modular Analyzer Series Cobas c502 Recalled by Roche Diagnostics...
The Issue: The Initial Cassette Volume Check (ICVC) is not activated on the cobas c 502...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merit Custom Syringe Kit Recalled by Merit Medical Systems, Inc. Due to The...
The Issue: The products are labeled as sterile but were not sterilized.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic MiniMed Paradigm Insulin Infusion Pumps Recalled by Medtronic...
The Issue: Medtronic is recalling the Medtronic MiniMed Paradigm Insulin Infusion Pumps...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monofilament and Multifilament Non-absorbable Steel Suture Recalled by...
The Issue: The products are being recalled because they did not meet minimum diameter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sutures Recalled by Teleflex Medical Due to The products are being recalled...
The Issue: The products are being recalled because they did not meet minimum needle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5/10/12 mm Weck¿ Vista" Universal Cannula Recalled by Teleflex Medical Due...
The Issue: Complaints were received of leakage of insufflation gas through the device,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5/10 Weck¿ Vista" Universal Balloon Open Access Port - Standard Length...
The Issue: Complaints were received of leakage of insufflation gas through the device,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sutures Recalled by Teleflex Medical Due to The products are being recalled...
The Issue: The products are being recalled because they did not meet minimum needle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5/10 mm Weck¿ Recalled by Teleflex Medical Due to Complaints were received...
The Issue: Complaints were received of leakage of insufflation gas through the device,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5/10/12 Weck¿ Vista" Universal Balloon Open Access Port Standard Length...
The Issue: Complaints were received of leakage of insufflation gas through the device,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Suture Recalled by Teleflex Medical Due to The products are being recalled...
The Issue: The products are being recalled because they did not meet minimum needle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sutures Recalled by Teleflex Medical Due to The products are being recalled...
The Issue: The products are being recalled because they did not meet minimum needle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Weck¿ Vista" Universal Laparoscopic Port Recalled by Teleflex Medical Due to...
The Issue: Complaints were received of leakage of insufflation gas through the device,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5/10/12MM X 100MM Weck¿ Vista" UNIVERSAL CONE OPEN ACCESS Recalled by...
The Issue: Complaints were received of leakage of insufflation gas through the device,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliSpace Portal (ISP) Recalled by Philips Medical Systems (Cleveland)...
The Issue: During SPECT reconstructions using Attenuation Correction and Scatter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 12mm Weck¿ Vista" Cannula-only Recalled by Teleflex Medical Due to...
The Issue: Complaints were received of leakage of insufflation gas through the device,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5/10/12 Weck¿ Vista" Universal Balloon Open Access Port Long Length...
The Issue: Complaints were received of leakage of insufflation gas through the device,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.