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. 1,006 recalls have been distributed to New Mexico in the last 12 months.
Showing 18521–18540 of 48,595 recalls
Recalled Item: Infinix-8000F with Catheterization Table CAT-850B or CAT-860B - Product...
The Issue: Bolts holding the longitudinal movement of catheterization tables may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infinix-8000V with Catheterization Table CAT-850B or CAT-860B - Product...
The Issue: Bolts holding the longitudinal movement of catheterization tables may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infinix-8000C with Catheterization Table CAT-850B or CAT-860B - Product...
The Issue: Bolts holding the longitudinal movement of catheterization tables may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PEPPERMINT LIP MOISTURIZER (oxybenzone (4%) and Octinoxate (7%) SPF 15...
The Issue: Superpotent drug: This lot of SPF containing lip balm contains up to 150% of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Daytrana (methylphenidate transdermal system) patches Recalled by Noven...
The Issue: Defective Delivery System: Out of specification for mechanical peel and shear.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Daytrana (methylphenidate transdermal system) patches Recalled by Noven...
The Issue: Defective Delivery System: Out of specification for mechanical peel and shear.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Carbidopa and Levodopa Tablets Recalled by Mayne Pharma Inc Due to Product...
The Issue: Product Mix-Up: A foreign tablet was found in bottle.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Daytrana (methylphenidate transdermal system) patches Recalled by Noven...
The Issue: Defective Delivery System: Out of specification for mechanical peel and shear.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Daytrana (methylphenidate transdermal system) patches Recalled by Noven...
The Issue: Defective Delivery System: Out of specification for mechanical peel and shear.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ReStructure VANILLA PROTEIN POWDER NET WT. 527G POUCH & 27G Recalled by New...
The Issue: The firm was notified that the labeling does not include the word milk on...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Merits E604 Pilot Navigator Stairlift - Product Usage: To transport Recalled...
The Issue: Pinion gear may disengage from track allowing lift to slip or jolt.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Portex Lumbar Puncture Tray. Anesthesia Conduction Kit. 4826PL-20 - Product...
The Issue: Cases of Portex¿ Lumbar Puncture Tray Child, SKU #4826PL-20 had been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ReWalk Personal 6.0 Recalled by Argo Medical Technologies Ltd Due to ReWalk...
The Issue: ReWalk Robotics received two complaints (one in the US; one in the Germany),...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: uDR 596i Digital Medical X-Ray Imaging System - Product Usage: Recalled by...
The Issue: Two issues were identified with the stationary x-ray system. 1. Some...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NAVIO Soft Tissue Protector Recalled by Smith & Nephew, Inc. Due to...
The Issue: Potential for the NAVIO Soft Tissue Protector to become stuck or bound to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gentell Hydrogel Ag 2x2 Recalled by Gentell, Inc Due to During an FDA audit,...
The Issue: During an FDA audit, it was discovered that the product was not properly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gentell Hydrogel Ag 4oz. Tube Recalled by Gentell, Inc Due to During an FDA...
The Issue: During an FDA audit, it was discovered that the product was not properly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gentell Hydrogel Ag 4x4 Recalled by Gentell, Inc Due to During an FDA audit,...
The Issue: During an FDA audit, it was discovered that the product was not properly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gentell Hydrogel Ag 4x8 Recalled by Gentell, Inc Due to During an FDA audit,...
The Issue: During an FDA audit, it was discovered that the product was not properly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica CH 930 Analyzer Recalled by Siemens Healthcare Diagnostics, Inc....
The Issue: Editing an assay Test Definition and switching to another assay s Test...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.