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. 2,605 recalls have been distributed to New Mexico in the last 12 months.
Showing 2901–2920 of 48,595 recalls
Recalled Item: Progressa Bed Surfaces Recalled by Baxter Healthcare Corporation Due to The...
The Issue: The air bladders inside the mattress may move out of position when the head...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter TruSystem 7500 Hybrid (FC) Recalled by Baxter Healthcare Corporation...
The Issue: There is a software issue which causes the upper back section to not be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter TruSystem 7500 Hybrid Plus (SC) Recalled by Baxter Healthcare...
The Issue: There is a software issue which causes the upper back section to not be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Floor mounting column TruSystem 7500 Recalled by Baxter Healthcare...
The Issue: There is a software issue which causes the upper back section to not be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Floor mounting column TS 7500 U Recalled by Baxter Healthcare...
The Issue: There is a software issue which causes the upper back section to not be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Mobile column TruSystem 7500 Recalled by Baxter Healthcare...
The Issue: There is a software issue which causes the upper back section to not be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zapzyt Recalled by Denison Pharmaceuticals, LLC Due to Chemical...
The Issue: Chemical Contamination: Presence of benzene.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Brand Name: Checkpoint Guardian Intraoperative Lead Product Name: Checkpoint...
The Issue: Adhesive on the back of the lead may not fully encapsulate the metallic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Checkpoint Guardian Intraoperative Lead Product Name: Checkpoint...
The Issue: Adhesive on the back of the lead may not fully encapsulate the metallic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COR Disposable Kit Recalled by DePuy Mitek, Inc., a Johnson & Johnson Co....
The Issue: Device is missing the pin in the graft loader component.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COR Disposable Kit Recalled by DePuy Mitek, Inc., a Johnson & Johnson Co....
The Issue: Device is missing the pin in the graft loader component.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HAZELNUT INTERNATIONAL delight COFFEE CREAMER 32 FL OZ (1 QT) Recalled by...
The Issue: The firm received complaints of spoilage and illness with the use of the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: CINNABON CLASSIC CINNAMON ROLL INTERNATIONAL delight COFFEE CREAMER 32 FL...
The Issue: The firm received complaints of spoilage and illness with the use of the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Vitality Recalled by One Source Nutrition, Inc, Due to Undeclared Sildenafil
The Issue: Marketed without an approved NDA/ANDA: Product found to be tainted with...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PHENYLephrine added to 0.9% sodium chloride Recalled by Central Admixture...
The Issue: Presence of Particulate Matter
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BD Connecta BD Luer-Lok 360 Recalled by BD SWITZERLAND SARL Due to Due to...
The Issue: Due to specific lots of luer-lok devices were shipped to the U.S. market...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Orthofix Pillar SA Ti Spacer System Intervertebral Body Fusion Spinal Device...
The Issue: The product is mislabeled with the incorrect anterior height of 10mm, but...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Helix Elite Inactivated Standard: Inactivated Influenza A/B and Respiratory...
The Issue: The RSV target may give a late Ct value and could potentially not pass QC.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Helix Elite" Inactivated Standard: Inactivated SARS-CoV-2 Whole Virus...
The Issue: The A549 human cell target (human cells for sample adequacy control) may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Wayson Hydrocolloid Models: 1) MJ BANDAGE HYDROCOLLOID HEEL OVAL 6CT...
The Issue: There is a potential for the sterility of the device to be compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.