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 21181–21200 of 48,595 recalls
Recalled Item: Neostigmine Methylsulfate Recalled by Premier Pharmacy Labs Inc Due to Lack...
The Issue: Lack of Assurance of Sterility: FDA inspection found insufficient...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SUCCINYLcholine Chloride Recalled by Premier Pharmacy Labs Inc Due to Lack...
The Issue: Lack of Assurance of Sterility: FDA inspection found insufficient...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SUCCINYLcholine Chloride Recalled by Premier Pharmacy Labs Inc Due to Lack...
The Issue: Lack of Assurance of Sterility: FDA inspection found insufficient...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Isoproterenol HCL in D5W (Non Sterile to Sterile) Recalled by Premier...
The Issue: Lack of Assurance of Sterility: FDA inspection found insufficient...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sodium Bicarbonate INJ 8.4% Recalled by Premier Pharmacy Labs Inc Due to...
The Issue: Lack of Assurance of Sterility: FDA inspection found insufficient...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Isoproterenol HCL in D5W Recalled by Premier Pharmacy Labs Inc Due to Lack...
The Issue: Lack of Assurance of Sterility: FDA inspection found insufficient...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Atropine Sulfate PF INJ Recalled by Premier Pharmacy Labs Inc Due to Lack of...
The Issue: Lack of Assurance of Sterility: FDA inspection found insufficient...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lidocaine 0.5%/Phenylephrine 0.75% P.F. INJ Recalled by Premier Pharmacy...
The Issue: Lack of Assurance of Sterility: FDA inspection found insufficient...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Penafiel Mineral Spring Water 600mL (20.3 FL OZ) and Penafiel Recalled by...
The Issue: Elevated levels of inorganic arsenic
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: da Vinci Surgical System Recalled by Intuitive Surgical, Inc. Due to One da...
The Issue: One da Vinci Xi Endoscope Controller in the field was improperly calibrated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lotemax (loteprednol etabonate ophthalmic gel 0.5%) Recalled by Bausch &...
The Issue: Failed Stability Specifications: Out of specification for viscosity.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CS100 Intra-Aortic Balloon Pump Recalled by Datascope Corp. Due to If...
The Issue: If battery maintenance is not performed appropriately, the battery may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products GLU Slides-Product Code:1707801. IVD VITROS...
The Issue: Potentially Biased Results using VITROS Chemistry Products GLU Slides
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CS100 Intra-Aortic Balloon Pump Recalled by Datascope Corp. Due to If...
The Issue: If battery maintenance is not performed appropriately, the battery may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Hybrid Intra-Aortic Balloon Pump (IABP) Recalled by Datascope...
The Issue: Battery short-run times and unanticipated stoppage may be due to user not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CS300 Intra-Aortic Balloon Pump Recalled by Datascope Corp. Due to If...
The Issue: If battery maintenance is not performed per instructions, the battery may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Rescue IABP Recalled by Datascope Corp. Due to If battery...
The Issue: If battery maintenance is not performed appropriately, the battery may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CS300 Intra-Aortic Balloon Pump Recalled by Datascope Corp. Due to If...
The Issue: If battery maintenance is not performed per instructions, the battery may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Babi.Plus 12.5 cm H2O Pressure Relief Manifold Catalog # 2691 Recalled by...
The Issue: Device vented gas below the stated pressure.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STANLEY Healthcare Arial 54315 Network Manager Recalled by Stanley Security...
The Issue: STANLEY Healthcare has received reports of outages on the Arial nurse call...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.