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. 1,862 recalls have been distributed to New Mexico in the last 12 months.
Showing 23061–23080 of 48,595 recalls
Recalled Item: Stationary Fluoroscopic X-ray System CombiDiagnost R90 Recalled by Philips...
The Issue: kV/mA lockin not functioning as specified which may result in the patient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Antacid Tablets Recalled by L. Perrigo Company Due to Presence of foreign...
The Issue: Presence of foreign substance: Product found to contain metal particles.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Megestrol Acetate Oral Suspension Recalled by Breckenridge Pharmaceutical,...
The Issue: Failed Stability Specifications: Out-of-Specification results obtained for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: IMRIS T2X table Recalled by Deerfield Imaging, Inc. Due to Table may drift...
The Issue: Table may drift in the roll position while in use
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMRIS ORT 300 Recalled by Deerfield Imaging, Inc. Due to Table may drift in...
The Issue: Table may drift in the roll position while in use
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMRIS ORT 100 table Recalled by Deerfield Imaging, Inc. Due to Table may...
The Issue: Table may drift in the roll position while in use
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMRIS ORT 200 Recalled by Deerfield Imaging, Inc. Due to Table may drift in...
The Issue: Table may drift in the roll position while in use
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: puriton EYE RELIEF DROPS Recalled by Kadesh International Due to...
The Issue: Non-Sterility: Product manufactured under non-sterile production conditions.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Duncan Hines Classic Classic Yellow cake mix 15.25oz. 12 retail Recalled by...
The Issue: positive finding of Salmonella in a retail sample
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Duncan Hines Classic Classic White cake mix 15.25oz. 12 retail Recalled by...
The Issue: positive finding of Salmonella in a retail sample
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Duncan Hines Signature Confetti Cake cake mix 15.25oz. 12 retail Recalled by...
The Issue: positive finding of Salmonella in a retail sample
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Duncan Hines Classic Butter Golden cake mix 15.25oz. 12 retail Recalled by...
The Issue: positive finding of Salmonella in a retail sample
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Optiflux F160NR Capillary High Flux Dialyzer Single Use Only Recalled by...
The Issue: Potential for external blood leaks from the dialyzer header
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: enVista One Piece Hydrophobic Acrylic Intraocular lens - Is indicated...
The Issue: Cosmetic imperfections on the surface of some lenses.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Captus 700 Thyroid Uptake System Recalled by Capintec Inc Due to There is a...
The Issue: There is a potential for the spring arm failure as a result of a broken...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Captus 3000 Thyroid Uptake System Recalled by Capintec Inc Due to There is a...
The Issue: There is a potential for the spring arm failure as a result of a broken...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Curaplex Epi Kit NOT FOR IV USE Recalled by Bound Tree Medical, LLC Due to...
The Issue: Labeling Incorrect Instructions: This recall has been initiated because the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Curaplex Epi Safe Kit Recalled by Bound Tree Medical, LLC Due to Labeling...
The Issue: Labeling Incorrect Instructions: This recall has been initiated because the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: curaplex Epi Safe Administration and Training Kits Recalled by Bound Tree...
The Issue: Labeling Incorrect Instructions: This recall has been initiated because the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: curaplex Epi Safe Kit Recalled by Bound Tree Medical, LLC Due to Labeling...
The Issue: Labeling Incorrect Instructions: This recall has been initiated because the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.