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. 2,605 recalls have been distributed to New Mexico in the last 12 months.
Showing 3141–3160 of 27,850 recalls
Recalled Item: AET36 ANESTH EXT SET - Anesthesia Extension Set - Normally Closed Dual...
The Issue: Potential for product leakage from the Spin Lock Connector on the distal end...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ViewPoint Recalled by GE Healthcare GmbH Due to The National Institute of...
The Issue: The National Institute of Standards and Technology (NIST) has identified in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biolox Option Taper Sleeve Recalled by Zimmer GmbH Due to Mislabeling
The Issue: Mislabeled: Incorrect sleeve in the packaging. The outer packaging is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Blood Pressure Module BPM3 TM-2917B (Spare Part Numbers 191378 or Recalled...
The Issue: Machines equipped with BPM3 Blood Pressure Modules (Blood pressure monitor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biolox Option Taper Sleeve Recalled by Zimmer GmbH Due to Mislabeling
The Issue: Mislabeled: Incorrect sleeve in the packaging. The outer packaging is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Allura Xper systems (R8.1 with Poly-G Stand) Interventional...
The Issue: A half-threaded bolt was included in the LTE kits instead of the correct...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAKO Integrated Cutting System (MICS) HANDPIECE Recalled by Howmedica...
The Issue: Stryker has identified an issue with the characterization process that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pacemaker Recalled by American Contract Systems, Inc. Due to ACS identified...
The Issue: ACS identified that due to an inoperable chart recorder, humidity readings...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biodesign Inguinal Hernia Graft C-IHM-10X15 - To reinforce soft tissues...
The Issue: Products expire prior to the expiration date printed on the product labeling
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hand Pack Recalled by American Contract Systems, Inc. Due to ACS identified...
The Issue: ACS identified that due to an inoperable chart recorder, humidity readings...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biodesign Fistula Plug C-FPB-0.7 - For implantation to reinforce soft...
The Issue: Products expire prior to the expiration date printed on the product labeling
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vaginal Delivery Recalled by American Contract Systems, Inc. Due to ACS...
The Issue: ACS identified that due to an inoperable chart recorder, humidity readings...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IR Procedure Pack Recalled by American Contract Systems, Inc. Due to ACS...
The Issue: ACS identified that due to an inoperable chart recorder, humidity readings...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nasal Sinus Pack Recalled by American Contract Systems, Inc. Due to ACS...
The Issue: ACS identified that due to an inoperable chart recorder, humidity readings...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PACEMAKER PACK Recalled by American Contract Systems, Inc. Due to ACS...
The Issue: ACS identified that due to an inoperable chart recorder, humidity readings...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Neuro Vascular Recalled by American Contract Systems, Inc. Due to ACS...
The Issue: ACS identified that due to an inoperable chart recorder, humidity readings...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endovascular AAA Pack Recalled by American Contract Systems, Inc. Due to ACS...
The Issue: ACS identified that due to an inoperable chart recorder, humidity readings...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bilateral Tubal Ligation Pack Recalled by American Contract Systems, Inc....
The Issue: ACS identified that due to an inoperable chart recorder, humidity readings...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biodesign Recto-Vaginal Fistula Plug RVP-0.2 - For implantation to reinforce...
The Issue: Products expire prior to the expiration date printed on the product labeling
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biodesign Fistula Plug C-FPS-0.7-2 - For implantation to reinforce soft...
The Issue: Products expire prior to the expiration date printed on the product labeling
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.