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. 942 recalls have been distributed to New Mexico in the last 12 months.
Showing 38561–38580 of 48,595 recalls
Recalled Item: FORUM Archive and Viewer Recalled by Carl Zeiss Meditec AG Due to Software...
The Issue: Software defect in the FORUM Viewer versions 3.1 and 3.2 which may lead to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Restoris Partial Knee Application (PKA) RIO (TGS 2.0). For use Recalled by...
The Issue: When using the MAKOplasty partial knee Arthroplasty application, the burr...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Go Raw Organic Spice Seed Mix Recalled by Freeland Foods Inc. Due to...
The Issue: CFIA notified firm of positive finding of Salmonella in Go Raw Spicy Seed...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Go Raw 100% Organic Sunflower Seeds Recalled by Freeland Foods Inc. Due to...
The Issue: CFIA notified firm of positive finding of Salmonella in Go Raw Spicy Seed...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: DynaLOC Breast Interventional Planning Software Versions 3.1 and 3.2...
The Issue: A device malfunction may cause the biopsy needle to fail to reach the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens LANTIS Oncology Information System Servers Recalled by Siemens...
The Issue: There is a potential safety risk when using LANTIS server software with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merge Hemo Recalled by Merge Healthcare, Inc. Due to A system freeze-up of...
The Issue: A system freeze-up of the Merge Hemo system, that included the PHASEIN End...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aquarius iNtuition Client Viewer. Findings Workflow module Recalled by...
The Issue: Software anomaly related to RECIST1.1 target lesion evaluation criteria in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hemodialysis Catheters and PICCs: Product identification: MCDLTSL24P (SF X...
The Issue: Drug products contained within the kits may have been rendered ineffective...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Levetiracetam Recalled by Sun Pharma Global Fze Due to Failed Dissolution...
The Issue: Failed Dissolution Specifications: 6 month time point.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ketorolac Tromethamine Ophthalmic Solution Recalled by Sun Pharma Global Fze...
The Issue: Presence of Particulate Matter: lot is not meeting the specification limit...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Avastin (Bevacizumab) 1.25 mg/0.05 mL syringe Recalled by Pacifico National,...
The Issue: Non-Sterility: Product tested positive for bacterial contamination.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 0.9% Sodium Chloride Injection Recalled by Hospira Inc. Due to Presence of...
The Issue: Presence of Particulate Matter; Hospira has identified the particulate as a...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Avastin (Bevacizumab) 2 mg/0.08 mL syringe Recalled by Pacifico National,...
The Issue: Non-Sterility: Product tested positive for bacterial contamination.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ADVIA Chemistry Systems Drug Calibrator I Recalled by Siemens Healthcare...
The Issue: Incorrect calibrator lot values were assigned for ADVIA Chemistry Systems...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KimVent Wet Pak Recalled by Halyard Health Due to Defect: A hole or crack...
The Issue: Defect: A hole or crack was found which may cause air to leak.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Brainlab Offset Cup Impactor Universal. Part of the Brainlab Recalled by...
The Issue: The recommended sterilization and drying parameters are not effective to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis One Recalled by Siemens Medical Solutions USA, Inc Due to The...
The Issue: The possibility exists that the monitor may fail and requires a power circle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KimVent Closed Suction System for Adults Recalled by Halyard Health Due to...
The Issue: Defect: A hole or crack was found which may cause air to leak.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BodyGuard 323 pump Recalled by CME America, LLC Due to CME America is...
The Issue: CME America is recalling the BodyGuard and BodyGuard 323 Infusion pumps due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.