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. 2,535 recalls have been distributed to New Mexico in the last 12 months.

48,595 total recalls
2,535 in last 12 months

Showing 1094110960 of 48,595 recalls

DrugSeptember 13, 2022· Lupin Pharmaceuticals Inc.

Recalled Item: Lisinopril Tablets USP Recalled by Lupin Pharmaceuticals Inc. Due to Foreign...

The Issue: Presence of Foreign Substance: Foreign material (metal piece) embedded in...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 9, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE PRE-OP CHG BATHING KIT Reorder #: P164756 Recalled by MEDLINE...

The Issue: Adult Blood Culture Collect kit and Pre-Op Changing Bathing Kit contain an...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 9, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE PHERIPHERAL BLOOD CULTURE DRAW Recalled by MEDLINE INDUSTRIES, LP -...

The Issue: Adult Blood Culture Collect kit and Pre-Op Changing Bathing Kit contain an...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 9, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE BLOOD CLUTURE KIT Recalled by MEDLINE INDUSTRIES, LP - Northfield...

The Issue: Adult Blood Culture Collect kit and Pre-Op Changing Bathing Kit contain an...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 9, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE ADLT BLOOD CLUTURE COLLECT KIT Recalled by MEDLINE INDUSTRIES, LP -...

The Issue: Adult Blood Culture Collect kit and Pre-Op Changing Bathing Kit contain an...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 9, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE 24 BLOOD CLUTURE KIT Recalled by MEDLINE INDUSTRIES, LP - Northfield...

The Issue: Adult Blood Culture Collect kit and Pre-Op Changing Bathing Kit contain an...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 8, 2022· Abbott Vascular

Recalled Item: Product/Part: MitraClip G4 CDS NT REPAIR-MR Clinical/CDS0704-NT Recalled by...

The Issue: An increase in clip locking malfunctions, Establish Final Arm Angle and Clip...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 8, 2022· Abbott Vascular

Recalled Item: Product/Part: MitraClip XTR Clip Delivery System US/CDS0601-XTR Recalled by...

The Issue: An increase in clip locking malfunctions, Establish Final Arm Angle and Clip...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 8, 2022· Abbott Vascular

Recalled Item: Product/Part: MitraClip NTR Clip Delivery System US/CDS0601-NTR Recalled by...

The Issue: An increase in clip locking malfunctions, Establish Final Arm Angle and Clip...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 7, 2022· Johnson & Johnson Surgical Vision, Inc.

Recalled Item: THERMOCOOL SMARTTOUCH SF Bi-Directional Navigation Catheter Recalled by...

The Issue: Manufacturing error resulted in potential contamination of Bi-Directional...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 7, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: CENTURION SnagFree Chest Tube insertion Tray Recalled by MEDLINE INDUSTRIES,...

The Issue: One lot of chest tube insertion trays, containing a silk suture component...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 7, 2022· BALT USA, LLC

Recalled Item: Optima Coil System Model Number OPTI0208CSS10 Recalled by BALT USA, LLC Due...

The Issue: Product pouch label does not match up with carton label

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 6, 2022· Philips Respironics, Inc.

Recalled Item: DreamWisp Nasal Mask with Over the Nose Cushion Recalled by Philips...

The Issue: No contraindication/warning regarding magnetic components in CPAP masks for...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 6, 2022· Philips Respironics, Inc.

Recalled Item: Wisp and Wisp Youth Nasal Mask Recalled by Philips Respironics, Inc. Due to...

The Issue: No contraindication/warning regarding magnetic components in CPAP masks for...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 6, 2022· Philips Respironics, Inc.

Recalled Item: Philips Respironics DreamWear Full Face Mask Recalled by Philips...

The Issue: No contraindication/warning regarding magnetic components in CPAP masks for...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 6, 2022· Philips Respironics, Inc.

Recalled Item: Therapy Mask 3100 NC/SP Recalled by Philips Respironics, Inc. Due to No...

The Issue: No contraindication/warning regarding magnetic components in CPAP masks for...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 6, 2022· Philips Respironics, Inc.

Recalled Item: Philips Respironics Amara View Minimal Contact Full-Face Mask Recalled by...

The Issue: No contraindication/warning regarding magnetic components in CPAP masks for...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 2, 2022· Baxter Healthcare Corporation

Recalled Item: Starling Monitor Recalled by Baxter Healthcare Corporation Due to Labeling...

The Issue: Labeling has incorrect or incomplete Unique Device Identification (UDI)...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing
Medical DeviceSeptember 2, 2022· LUMINOSTICS, INC dba CLIP HEALTH

Recalled Item: Clip COVID Rapid Antigen Test Kit (25-pack) Recalled by LUMINOSTICS, INC dba...

The Issue: COVID test kit shelf life was periodically extended, as real-time stability...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 1, 2022· OMM Imports, Inc. dba Zero Gravity

Recalled Item: Recreo Hair Growth Laser Comb Recalled by OMM Imports, Inc. dba Zero Gravity...

The Issue: The firm distributed the laser products without affixing the warning,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing