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. 2,025 recalls have been distributed to New Mexico in the last 12 months.
Showing 5841–5860 of 27,850 recalls
Recalled Item: MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter Recalled...
The Issue: Catheter center lumen was found to have an occlusion in the tip of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter Recalled...
The Issue: Catheter center lumen was found to have an occlusion in the tip of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter Recalled...
The Issue: Catheter center lumen was found to have an occlusion in the tip of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter Recalled...
The Issue: Catheter center lumen was found to have an occlusion in the tip of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACROBAT SUV Vacuum Off-Pump System Recalled by Maquet Cardiovascular, LLC...
The Issue: The Standard Blade may not securely latch onto the Activator Drive. This may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACCESSRAIL Platform (Standard Blade) Part Number SB-1000 Recalled by Maquet...
The Issue: The Standard Blade may not securely latch onto the Activator Drive. This may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACROBAT-i Vacuum Stabilizer System Recalled by Maquet Cardiovascular, LLC...
The Issue: The Standard Blade may not securely latch onto the Activator Drive. This may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACROBAT V Vacuum Off-Pump System Recalled by Maquet Cardiovascular, LLC Due...
The Issue: The Standard Blade may not securely latch onto the Activator Drive. This may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: stryker 3.0MM Precision Neuro Match Head Recalled by Stryker Corporation Due...
The Issue: There is potential the device inside the package may not match the product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: stryker 3.0MM Neuro Match Head Recalled by Stryker Corporation Due to There...
The Issue: There is potential the device inside the package may not match the product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The 3.0MM Neuro Match Head Soft Touch bur (5820-107-030) is Recalled by...
The Issue: There is potential the device inside the package may not match the product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Periarticular Locking Plate (ZPLP) Distal Lateral Femoral Plate 6...
The Issue: Thread form issue of the locking holes in that the locking screws would not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fargo Ortho-K Lens Recalled by PARAGON VISION SCIENCES, Inc Due to...
The Issue: Manufactured lenses are not covered by existing FDA approval
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ISee Ortho-K Lens Recalled by PARAGON VISION SCIENCES, Inc Due to...
The Issue: Manufactured lenses are not covered by existing FDA approval
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: YAMATO PLUS IAB Recalled by Datascope Corp. Due to During IAB catheter...
The Issue: During IAB catheter insertion, the introducer dilator may fracture at the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Equipment and table drapes: (1) Ecolab Banded Bag with Rubberband and Tape...
The Issue: Certain lots of the products have a Naphthalene odor.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEGA 8Fr. IAB Recalled by Datascope Corp. Due to During IAB catheter...
The Issue: During IAB catheter insertion, the introducer dilator may fracture at the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: REINFORCED INTRODUCER SET Recalled by Datascope Corp. Due to During IAB...
The Issue: During IAB catheter insertion, the introducer dilator may fracture at the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Equipment and table drapes and Surgical Room Turnover (SRT) Kits: Recalled...
The Issue: Certain lots of the products have a Naphthalene odor.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEGA 7.5Fr.IAB Recalled by Datascope Corp. Due to During IAB catheter...
The Issue: During IAB catheter insertion, the introducer dilator may fracture at the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.