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. 2,606 recalls have been distributed to New Mexico in the last 12 months.
Showing 901–920 of 48,595 recalls
Recalled Item: Sticker label (for Loose Bulk - yellow peaches): 4044 Recalled by Moonlight...
The Issue: Potential contamination with Listeria monocytogenes.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Lisdexamfetamine Dimesylate Capsules Recalled by SUN PHARMACEUTICAL...
The Issue: Failed Dissolution Specifications: An out of specification results observed...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lisdexamfetamine Dimesylate Capsules Recalled by SUN PHARMACEUTICAL...
The Issue: Failed Dissolution Specifications: An out of specification results observed...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lisdexamfetamine Dimesylate Capsules Recalled by SUN PHARMACEUTICAL...
The Issue: Failed Dissolution Specifications: An out of specification results observed...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lisdexamfetamine Dimesylate Capsules Recalled by SUN PHARMACEUTICAL...
The Issue: Failed Dissolution Specifications: An out of specification results observed...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lisdexamfetamine Dimesylate Capsules Recalled by SUN PHARMACEUTICAL...
The Issue: Failed Dissolution Specifications: An out of specification results observed...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lisdexamfetamine Dimesylate Capsules Recalled by SUN PHARMACEUTICAL...
The Issue: Failed Dissolution Specifications: An out of specification results observed...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lisdexamfetamine Dimesylate Capsules Recalled by SUN PHARMACEUTICAL...
The Issue: Failed Dissolution Specifications: An out of specification results observed...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Welch Allyn INF BAG Recalled by Baxter Healthcare Corporation Due to...
The Issue: Replacement bladder kit for the Welch Allyn two-piece reusable blood...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reagent Kits/ containing flow cells Recalled by Illumina, Inc. Due to An...
The Issue: An instrument intended for sequencing DNA libraries with in vitro diagnostic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 0.9% SODIUM CHLORIDE Injection Recalled by Otsuka ICU Medical LLC Due to...
The Issue: Lack of Assurance of Sterility: Potential for flexible container leaks.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: MEDLINE PERFUSION SYRINGE Recalled by Medline Industries, LP Due to Medline...
The Issue: Medline Industries, LP is issuing a recall for specific item(s) and lot(s)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hemodialysis System Recalled by Nipro Medical Corporation Due to Screw may...
The Issue: Screw may loosen or fallout of Hemodialysis system
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: EDAN Product Name: Fetal Monitor Model/Catalog Number: F2...
The Issue: As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: EDAN Product Name: Vital Signs Monitor Model/Catalog Number:...
The Issue: As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: EDAN Product Name: Central Monitoring System Model/Catalog...
The Issue: As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: EDAN Product Name: Vital Signs Monitor Model/Catalog Number:...
The Issue: As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: EDAN Product Name: Telemetry Transmitter Model/Catalog Number:...
The Issue: As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: EDAN Product Name: Patient Monitor Model/Catalog Number: iX10...
The Issue: As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: EDAN Product Name: Patient Monitor Model/Catalog Number: elite...
The Issue: As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.