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. 913 recalls have been distributed to New Mexico in the last 12 months.
Showing 44221–44240 of 48,595 recalls
Recalled Item: VITROS Chemistry Products CK Slides packaged as 300 slides/pack catalog...
The Issue: Ortho Clinical Diagnostics is recalling Slide Dispense cartridges used with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products ALKP Slides Recalled by Ortho-Clinical Diagnostics...
The Issue: Ortho Clinical Diagnostics is recalling Slide Dispense cartridges used with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products SALI Slides packaged as 90 slides/pack catalog...
The Issue: Ortho Clinical Diagnostics is recalling Slide Dispense cartridges used with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products PROT Slides packaged as 90 slides/pack catalog...
The Issue: Ortho Clinical Diagnostics is recalling Slide Dispense cartridges used with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Omnicycle Elite Recalled by Accelerated Care Plus Corporation Due to An...
The Issue: An anomaly in the firmware that may cause Omnicycle Elite to operate at a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes CMF Distraction System The product is intended for use Recalled by...
The Issue: The firm initiated a voluntary recall of the BC Distractor Body which is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The LIFEPAK 500 Automated External Defibrillator is a semi-automatic...
The Issue: The LIFEPAK 500 Automated External Defibrillator (AED) could be susceptible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arm & Hammer Baking Soda a) Net Wt. 1 LB. Recalled by Church & Dwight Inc...
The Issue: Church and Dwight Co., Inc. has initiated a recall for Sodium Bicarbonate,...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Pistachios Recalled by Hearthside Food Solutions LLC Due to One of our...
The Issue: One of our vendors, ARO Pistachio Inc., is issuing an FDA Class 2 Voluntary...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Bethel 30 capsules Recalled by Bethel Nutritional Consulting, Inc Due to...
The Issue: Marketed Without An Approved NDA/ANDA: FDA analysis found this product...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sodium Bicarbonate Powder Recalled by Church & Dwight Inc Due to Presence of...
The Issue: Presence of Foreign Substance: raw material recalled due to stainless steel...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sodium Bicarbonate Powder Recalled by Church & Dwight Inc Due to Presence of...
The Issue: Presence of Foreign Substance: raw material recalled due to stainless steel...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sodium Bicarbonate Powder Recalled by Church & Dwight Inc Due to Presence of...
The Issue: Presence of Foreign Substance: raw material recalled due to stainless steel...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sodium Bicarbonate Powder Recalled by Church & Dwight Inc Due to Presence of...
The Issue: Presence of Foreign Substance: raw material recalled due to stainless steel...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sodium Bicarbonate Powder Recalled by Church & Dwight Inc Due to Presence of...
The Issue: Presence of Foreign Substance: raw material recalled due to stainless steel...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Integra Licox Brain Tissue Oxygen Monitoring 1 x Complete Brain Recalled by...
The Issue: Integra LifeSciences Corporation has determined that there is a possibility...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Centricity PACS Workstation is intended for use as a Recalled by GE...
The Issue: GE has recently become aware of potential issues due to out of context...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Healthcare MobileDiagnostwDR system. Mobile Digital radiography...
The Issue: The Instructions for Use (IFU) for the MobileDiagnost wDR fails to comply...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sodium Bicarbonate Recalled by Church & Dwight Inc Due to Church and Dwight...
The Issue: Church and Dwight Co., Inc. has initiated a recall for Sodium Bicarbonate,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Flexible Medullary Reamer. Intended to be used to facilitate...
The Issue: Due to the coiled design for this product, the product is difficult to clean...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.