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. 2,020 recalls have been distributed to New Mexico in the last 12 months.
Showing 6501–6520 of 48,595 recalls
Recalled Item: Wash station: M1000 Wash Station Assembly & DITI Slide Recalled by Abbott...
The Issue: Products that were intended for export only which were not approved or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: In-vitro diagnostic kits: (1) Abbott Vysis MDM2 / CEP 12 FISH Probe Kit...
The Issue: Products that were intended for export only which were not approved or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Pyxis: MedStation ES Recalled by CareFusion 303, Inc. Due to Automated...
The Issue: Automated dispensing cabinets, running affected software, and Windows 10...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: To the Moon Capsules Recalled by Integrity Products Due to Undeclared Sildenafil
The Issue: Marketed Without an Approved NDA/ANDA: Products contain undeclared sildenafil.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HydrALAZINE Hydrochloride Tablets Recalled by Amerisource Health Services...
The Issue: Failed Impurities/Degradation Specifications: Out of Specification (OOS)...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: TING 1% Tolnaftate Athlete's Foot Spray Antifungal Spray Liquid Recalled by...
The Issue: Chemical Contamination; presence of benzene.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: RAM IT Recalled by Integrity Products Due to Undeclared Sildenafil
The Issue: Marketed Without an Approved NDA/ANDA: Products contain undeclared sildenafil.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lansoprazole Delayed-Release Capsules USP Recalled by NATCO Pharma Limited...
The Issue: CGMP Deviations: Inadequate induction sealing on bottles, capsules were...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Coffee 5 pound bags Recalled by House of Coffee Beans, Inc Due to potential...
The Issue: potential allergen contact with almonds, pecans and coconut.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Microalbumin Calibrator Series (mALB CAL)-IVD used to calibrate the...
The Issue: Microalbumin Calibrator Series, MA1567 & MA2426, is running with a negative...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Microalbumin Calibrator Series (mALB CAL)-IVD to calibrate the Microalbumin...
The Issue: Microalbumin Calibrator Series, MA1567 & MA2426, is running with a negative...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trumpet Recalled by Technicality Inc. Due to The Ring on the Trump Needle...
The Issue: The Ring on the Trump Needle Guide can detach when excessive pressure is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MINI STICK MAX 5F X 10 CM STIFF .018 NI/TU Recalled by Angiodynamics, Inc....
The Issue: Non-conformance may prevent the guidewire from passing through the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MINI STICK MAX 4F X 10 CM STIFF .018 SS/SS Recalled by Angiodynamics, Inc....
The Issue: Non-conformance may prevent the guidewire from passing through the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MINI STICK MAX 4F X 10CM STIFF .018 NI/TU ECHO Recalled by Angiodynamics,...
The Issue: Non-conformance may prevent the guidewire from passing through the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MINI STICK MAX 5F X 10 CM STD .018 SS/SS Recalled by Angiodynamics, Inc. Due...
The Issue: Non-conformance may prevent the guidewire from passing through the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MINI STICK MAX 5F X 10 CM STIFF .018 SS/PD Recalled by Angiodynamics, Inc....
The Issue: Non-conformance may prevent the guidewire from passing through the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MINI STICK MAX 4F X 10 CM STIFF .018 NI/TU Recalled by Angiodynamics, Inc....
The Issue: Non-conformance may prevent the guidewire from passing through the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MINI STICK MAX 4F X 10 CM STIFF .018 SS/PD Recalled by Angiodynamics, Inc....
The Issue: Non-conformance may prevent the guidewire from passing through the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MINI STICK MAX 5F X 15 CM STIFF .018 NI/TU Recalled by Angiodynamics, Inc....
The Issue: Non-conformance may prevent the guidewire from passing through the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.