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. 1,078 recalls have been distributed to New Mexico in the last 12 months.
Showing 8361–8380 of 48,595 recalls
Recalled Item: Safe Tussin PM Night Time Cough Relief (Cough Suppressant/Antihistamine)...
The Issue: CGMP Deviations: use of non-food grade lubricant in mixing vessel.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Tizanidine Tablets Recalled by Amerisource Health Services LLC Due to Failed...
The Issue: Failed Dissolution Specifications: this repackaged product was recalled by...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Tydemy (drospirenone Recalled by Lupin Pharmaceuticals Inc. Due to Failed...
The Issue: Failed Stability Specification and Failed Impurities/Degradation...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PANCREAZE (pancrelipase) Delayed-Release Capsules Recalled by Vivus, Inc....
The Issue: Failed Stability Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Safe Tussin DM Cough + Chest Congestion (Dextromethorphan HBr/ Cough...
The Issue: CGMP Deviations: use of non-food grade lubricant in mixing vessel.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Diclofenac Sodium Topical Solution USP Recalled by ALEMBIC PHARMACEUTICALS,...
The Issue: Defective Delivery System
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: STATCLAVE G4 Chamber Autoclave -Tabletop steam sterilizer intended for use...
The Issue: The STATCLAVE G4 is a dynamic air removal (prevacuum) tabletop steam...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gore Tips Set Device Recalled by Creganna Medical Devices Due to Three lots...
The Issue: Three lots of product may be labeled with an incorrect expiration day
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INFX-8000C XGCP-930AA TABLE SIDE CONSOLE Recalled by Canon Medical System,...
The Issue: The C-arm, used to set the position and angle of the x-ray exposure field,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STATCLAVE G4 Chamber Autoclave -Tabletop steam sterilizer intended for use...
The Issue: The STATCLAVE G4 is a dynamic air removal (prevacuum) tabletop steam...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Randox Liquid Urine Control Level 2- intended for in vitro diagnostic use...
The Issue: (1) There is vial to vial variation resulting in some vials recovering...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trader Joe s Organic Tropical Fruit Blend Pineapple Recalled by Scenic Fruit...
The Issue: Potential for contamination with Listeria monocytogenes. Pineapples are...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Tizanidine Tablets USP Recalled by Dr Reddy's Laboratories Limited Due to...
The Issue: Failed dissolution specification: Out of specification results observed in...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cadia - Organic Pineapple Frozen Fruit Recalled by Scenic Fruit Company, LLC...
The Issue: Potential for contamination with Listeria monocytogenes. Pineapples are...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Ringed DxI Reaction Vessels (RVs) Recalled by Beckman Coulter, Inc. Due to...
The Issue: Beckman Coulter, Inc. is recalling Ringed DxI Reaction Vessels (RVs) as part...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARTIS icono floor-Angiography systems developed for single and biplane...
The Issue: Due to a hardware issue in the cable connectors of the system generator, a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARTIS icono biplane -Angiography systems developed for single and biplane...
The Issue: Due to a hardware issue in the cable connectors of the system generator, a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ProPlan CMF Patient-Specific Guide Recalled by Materialise N.V. Due to Wrong...
The Issue: Wrong versions of guides 3A and 3B (Patient Specific) were shipped prior to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARTIS pheno-Angiography systems developed for single and biplane diagnostic...
The Issue: Due to a hardware issue in the cable connectors of the system generator, a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NovaPlus Infant Heel Warmer Recalled by Cardinal Health 200, LLC Due to...
The Issue: Cardinal Health has received an increase in burst/leaking complaints from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.