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 9621–9640 of 48,595 recalls
Recalled Item: CombiDiagnost R90 R.1.0 Recalled by Philips North America Due to Philips has...
The Issue: Philips has identified a compliance issue where ProxiDiagnost N90 R.1.0,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ProxiDiagnost N90 R.1.0 Recalled by Philips North America Due to Philips has...
The Issue: Philips has identified a compliance issue where ProxiDiagnost N90 R.1.0,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centurion CirClamp with 1.3cm Bell & Insert Reprocessed Recalled by MEDLINE...
The Issue: The CirClamp subassembly found in the kit was the incorrect size.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SafeLight Fiber Optic Cable: Clear Recalled by Stryker Corporation Due to...
The Issue: Fiber optic cables assembled with not enough epoxy on the proximal end,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NanoKnife 5-Probe Procedure Pack 15 cm - Activation. Indicated for Recalled...
The Issue: Not programmed in accordance with specification. The programming affects the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alprazolam Tablets Recalled by Breckenridge Pharmaceutical, Inc Due to CGMP...
The Issue: CGMP Deviations: Potential risk of Cross Contamination
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Alprazolam Tablets Recalled by Breckenridge Pharmaceutical, Inc Due to CGMP...
The Issue: CGMP Deviations: Potential risk of Cross Contamination
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Clobazam Tablets Recalled by Breckenridge Pharmaceutical, Inc Due to CGMP...
The Issue: CGMP Deviations: Potential risk of Cross Contamination
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Alprazolam Tablets Recalled by Breckenridge Pharmaceutical, Inc Due to CGMP...
The Issue: CGMP Deviations: Potential risk of Cross Contamination
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Alprazolam Tablets Recalled by Breckenridge Pharmaceutical, Inc Due to CGMP...
The Issue: CGMP Deviations: Potential risk of Cross Contamination
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Calcitonin Salmon Nasal Spray Recalled by Endo Pharmaceuticals, Inc. Due to...
The Issue: Failed Impurities/Degradation Specifications and Subpotent Drug: High Out of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Clobazam Tablets Recalled by Breckenridge Pharmaceutical, Inc Due to CGMP...
The Issue: CGMP Deviations: Potential risk of Cross Contamination
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Brimonidine Tartrate Ophthalmic Solution 0.15% Recalled by Apotex Corp. Due...
The Issue: Lack of sterility assurance: Cracks have developed in some of the units caps...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Heparin Sodium Recalled by B. Braun Medical Inc Due to Subpotent Drug: low...
The Issue: Subpotent Drug: low Anti-Factor IIa potency.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: DG Health brand Sugar Free Daily Fiber in 10 oz. Recalled by Dollar General...
The Issue: Product is missing warning declaration that it contains phenylalanine.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Stryker Color Cuff Non-Sterile Disposable Tourniquet Cuff -NS DISP 18X4...
The Issue: Not able to achieve desired pressure and not holding pressure result from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trilogy EV300 Portable Electric Ventilator Recalled by Philips Respironics,...
The Issue: The accuracy of delivered oxygen may deviate below the required tolerance of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Color Cuff Non-Sterile Disposable Tourniquet Cuff -NS DISP 34X4...
The Issue: Not able to achieve desired pressure and not holding pressure result from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Express Mini 500 Dry Seal Chest Drain Recalled by Atrium Medical Corporation...
The Issue: The Instructions for Use (IFU) for the Pneumostat Chest Drain Valve and the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CAPIOX RX15 Hollow Fiber Oxygenator Recalled by Terumo Cardiovascular...
The Issue: Some Capiox NX, RX and FX Oxygenators may contain an arterial thermistor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.