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. 1,078 recalls have been distributed to New Mexico in the last 12 months.
Showing 6801–6820 of 48,595 recalls
Recalled Item: Impella catheters - Intravascular micro axial blood pumps that support...
The Issue: New warnings are being added to the Instructions for Use for all affected...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Senographe Pristina Recalled by GE Medical Systems, SCS Due to X-ray...
The Issue: X-ray exposure termination audible signal on Senographe Pristina with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Power Knee Recalled by Ossur H / F Due to Knee batteries may need...
The Issue: Knee batteries may need replacement with conforming batteries to ensure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Robitussin Honey CF Max Nighttime Adult (Acetaminophen 650 mg Recalled by...
The Issue: Microbial Contamination of Non-Sterile Products
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Benzonatate Capsules Recalled by Amerisource Health Services LLC Due to...
The Issue: Superpotent drug: Assay results were slightly above specification at the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Divalproex Sodium Extended-release Tablets Recalled by Amneal...
The Issue: Failed dissolution specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Robitussin Honey CF Max Non-Drowsy Adult (Acetaminophen 650mg Recalled by...
The Issue: Microbial Contamination of Non-Sterile Products
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HRIS ACET CUP CUT TIP 32X140 Part Number: 6210-5-200rker. single-use...
The Issue: Failed to meet the acceptance criteria for the seal integrity and/or package...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HRIS ACET CUP CUT TIP 26X140 Part Number: 6210-5-100. single-use Recalled by...
The Issue: Failed to meet the acceptance criteria for the seal integrity and/or package...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ELEOS COLLAR STEM Recalled by Onkos Surgical, Inc. Due to Mislabeling
The Issue: Mislabeling of 13mm Modular Segmental Stem package (HC-13120-03M) which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ELEOS COLLAR STEM Recalled by Onkos Surgical, Inc. Due to Mislabeling
The Issue: Mislabeling of 13mm Modular Segmental Stem package (HC-13120-03M) which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HENRY SCHEIN¿ CRITERION¿ ANTI-FOG EARLOOP MASKS LEVEL 3 (BLUE) (item...
The Issue: Level 3 masks were produced on alternate non-validated production equipment...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE BLOOD CULTURE COLLECTION KIT Recalled by MEDLINE INDUSTRIES, LP -...
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: Sofsilk Braided Silk sutures: CS-211 SOFSILK* 4-0 BLK 45CM CVF21 Recalled by...
The Issue: Specific lots of sutures were sterilized with gamma doses that exceeded the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PATTERSON¿ PROCEDURE EARLOOP MASKS- ANTI-FOG Recalled by AMD Medicom Inc....
The Issue: Level 3 masks were produced on alternate non-validated production equipment...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE BLOOD CULTURE KIT Recalled by MEDLINE INDUSTRIES, LP - Northfield...
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: MEDLINE BLOOD CULTURE COLLECTION KIT Recalled by MEDLINE INDUSTRIES, LP -...
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: HENRY SCHEIN¿ CRITERION¿ EARLOOP MASKS LEVEL 3 (BLUE) (item code 570-2448)...
The Issue: Level 3 masks were produced on alternate non-validated production equipment...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Surgilon Braided Nylon sutures: 88861919-31 SURGILON* 4-0 BLK 7X75CMPCT...
The Issue: Specific lots of sutures were sterilized with gamma doses that exceeded the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE ADULT BLOOD CULTURE KIT Recalled by MEDLINE INDUSTRIES, LP -...
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.