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. 1,839 recalls have been distributed to New Mexico in the last 12 months.
Showing 25421–25440 of 48,595 recalls
Recalled Item: Loxapine Capsules Recalled by Mylan Institutional, Inc. (d.b.a. UDL...
The Issue: GMP Deviations: a recent FDA inspection of the manufacturing site revealed...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Loxapine Capsules Recalled by Mylan Institutional, Inc. (d.b.a. UDL...
The Issue: GMP Deviations: a recent FDA inspection of the manufacturing site revealed...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ampicillin and Sulbactam for Injection Recalled by AuroMedics Pharma LLC Due...
The Issue: Presence of Particulate Matter: confirmed customer report of the presence of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Piperacillin and Tazobactam for Injection Recalled by AuroMedics Pharma LLC...
The Issue: Presence of Particulate Matter: confirmed customer report for presence of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: IntelliVue MX40 Patient Monitor Recalled by Philips Electronics North...
The Issue: Five warning statements are missing from the instructions for use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliVue MX40 Patient Monitor Recalled by Philips Electronics North...
The Issue: Five warning statements are missing from the instructions for use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliVue MX40 Patient Monitor Recalled by Philips Electronics North...
The Issue: Five warning statements are missing from the instructions for use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliVue MX40 Patient Monitor Recalled by Philips Electronics North...
The Issue: Five warning statements are missing from the instructions for use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Elecsys Vitamin D total II Recalled by Roche Diagnostics Corporation Due to...
The Issue: The device may give a falsely elevated result that is non-reproducible. If...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Elecsys Vitamin D total II Recalled by Roche Diagnostics Corporation Due to...
The Issue: The device may give a falsely elevated result that is non-reproducible. If...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Revolution EVO Recalled by GE Healthcare Japan Corporation Due...
The Issue: GE Healthcare has identified that some CT systems may have a damaged cable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Optima CT660. The systems are intended for head Recalled by GE...
The Issue: GE Healthcare has identified that some CT systems may have a damaged cable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Optima CT540. The systems are intended for head Recalled by GE...
The Issue: GE Healthcare has identified that some CT systems may have a damaged cable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Optima CT660. Sold under the following product names: Recalled...
The Issue: GE Healthcare has identified that some CT systems may have a damaged cable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Docetaxel injection concentrate Recalled by Sanofi-Aventis U.S. LLC Due to...
The Issue: Superpotent drug: over-concentrated vials of Docetaxel injection concentrate...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Riomet (metformin hydrochloride oral solution) Recalled by Sun...
The Issue: Labeling: Not Elsewhere Classified: Sun Pharma has decided to initiate this...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BOX KITDE0108 BYPASS KIT LUEBECK ( KITDE0108) Product Usage: The Recalled by...
The Issue: Device may be missing a sled component. The sled component is responsible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ABX Pentra Micro ALBUMIN 2 CP Recalled by Horiba Instruments, Inc dba Horiba...
The Issue: When the ABX Pentra Micro ALBUMIN 2 CP (ALBT2) Reagent 2 is sampled and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BOX1073076GASB1 BBR GASTRIC BYPASS S(Item Code BOX1073076GASB1 BBR GASTRIC...
The Issue: Device may be missing a sled component. The sled component is responsible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (1) BOX BOX1073180 APPE1 APPENDIX KIT ZAMS (Item Code BOX1073180) Recalled...
The Issue: Device may be missing a sled component. The sled component is responsible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.