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. 958 recalls have been distributed to New Mexico in the last 12 months.

48,595 total recalls
958 in last 12 months

Showing 36961–36980 of 48,595 recalls

Medical DeviceMay 28, 2015· American Medical Systems Innovation Center - Silicon Valley

Recalled Item: 1X1 Cleaving Tiles Recalled by American Medical Systems Innovation Center -...

The Issue: validation data related to cleaning instructions and sterilization methods...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2015· American Medical Systems Innovation Center - Silicon Valley

Recalled Item: Tool Recalled by American Medical Systems Innovation Center - Silicon Valley...

The Issue: validation data related to cleaning instructions and sterilization methods...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2015· Cook Inc.

Recalled Item: Flexor RTPS Guiding Sheath Product Usage: The Flexor RTPS Guiding Recalled...

The Issue: Cook Inc. is initiating a voluntary recall of the Ring Transjugular...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2015· American Medical Systems Innovation Center - Silicon Valley

Recalled Item: Sureflex 200 Lithotripsy Fiber Recalled by American Medical Systems...

The Issue: validation data related to cleaning instructions and sterilization methods...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2015· American Medical Systems Innovation Center - Silicon Valley

Recalled Item: Sureflex 550 Lithotripsy Fiber Recalled by American Medical Systems...

The Issue: validation data related to cleaning instructions and sterilization methods...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2015· American Medical Systems Innovation Center - Silicon Valley

Recalled Item: Fiber Stripper Recalled by American Medical Systems Innovation Center -...

The Issue: validation data related to cleaning instructions and sterilization methods...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2015· American Medical Systems Innovation Center - Silicon Valley

Recalled Item: Tool Recalled by American Medical Systems Innovation Center - Silicon Valley...

The Issue: validation data related to cleaning instructions and sterilization methods...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2015· American Medical Systems Innovation Center - Silicon Valley

Recalled Item: Stripper Recalled by American Medical Systems Innovation Center - Silicon...

The Issue: validation data related to cleaning instructions and sterilization methods...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2015· Synthes, Inc.

Recalled Item: Reamer / Irrigator / Aspirator (RIA): RIA Drive Shafts Recalled by Synthes,...

The Issue: It was reported that the RIA Drive Shaft, Tube Assembly, and Reamer Head...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 27, 2015· Bard Access Systems

Recalled Item: PowerPICC SOLO Catheter with Sherlock 3CG TPS Stylet 4F Maximal Recalled by...

The Issue: Bard Access Systems is recalling PowerPICC Solo Catheter Kits due to...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing
Medical DeviceMay 27, 2015· Bard Access Systems

Recalled Item: PowerPICC SOLO Catheter with Tip Location System (TLS) Stylet 4F Recalled by...

The Issue: Bard Access Systems is recalling PowerPICC Solo Catheter Kits due to...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing
Medical DeviceMay 27, 2015· Bard Access Systems

Recalled Item: PowerPICC SOLO2 Catheter 4F Maximal Barrier Tray with Microintroducer...

The Issue: Bard Access Systems is recalling PowerPICC Solo Catheter Kits due to...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing
Medical DeviceMay 27, 2015· Integra LifeSciences Corp.

Recalled Item: Integra Camino Intracranial Pressure Monitoring Catheter with Licox IMC Bolt...

The Issue: Integra LifeSciences is recalling the Camino Intracranial Pressure...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 27, 2015· Musculoskeletal Transplant Foundation, Inc.

Recalled Item: Allofix Insertion Kit Recalled by Musculoskeletal Transplant Foundation,...

The Issue: Musculoskeletal Transplant Foundation is recalling a certain lot of Allofix...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 27, 2015· Synthes, Inc.

Recalled Item: DePuy Synthes 6.5 mm Titanium Recon Screws w/T25 Stardrive (70mm Recalled by...

The Issue: certain lots of the Titanium Recon Screws (6.5mm ) were found to contain the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 27, 2015· Bard Access Systems

Recalled Item: PowerPICC SOLO Catheter with Sherlock 3CG (TPS) Stylet 5F Maximal Recalled...

The Issue: Bard Access Systems is recalling PowerPICC Solo Catheter Kits due to...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing
DrugMay 27, 2015· Bracco Diagnostic Inc

Recalled Item: E-Z-CAT Dry Barium Sulfate for Suspension (2% w/w after mixing) Recalled by...

The Issue: Failed stability specifications:This recall has been initiated due to out of...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
FoodMay 27, 2015· Novacare, LLC

Recalled Item: Glucosamine 750 mg 120 ct Recalled by Novacare, LLC Due to TSN Labs is...

The Issue: TSN Labs is conducting a field action on Glucosamine 750 mg 120 ct due to...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 26, 2015· Bausch & Lomb Surgical, Inc.

Recalled Item: Bausch & Lomb SoFlex SE Foldable intraocular Lens Product Usage: Recalled by...

The Issue: Haptics breaking during lens loading and insertion.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 26, 2015· Smiths Medical ASD, Inc.

Recalled Item: CADD¿- Solis Ambulatory Infusion Pump Recalled by Smiths Medical ASD, Inc....

The Issue: Smiths Medical has become aware of an issue with an intermittent occurrence...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing