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. 1,872 recalls have been distributed to New Mexico in the last 12 months.
Showing 17681–17700 of 27,850 recalls
Recalled Item: Optima MR750 3.0T Product Usage: The Optima MR450 1.5T system Recalled by GE...
The Issue: Possible incorrect wiring of the Uninterruptable Power Supply, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Phoenix PMIC-107 Recalled by Becton Dickinson & Co. Due to BD has...
The Issue: BD has recently confirmed quality control failures, related to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brivo MR355 Recalled by GE Medical Systems, LLC Due to Possible incorrect...
The Issue: Possible incorrect wiring of the Uninterruptable Power Supply, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Signa PET/MR (K163619 Recalled by GE Medical Systems, LLC Due to Possible...
The Issue: Possible incorrect wiring of the Uninterruptable Power Supply, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Discovery MR750 3.0T Product Usage: Intended use: The Discovery MR750...
The Issue: Possible incorrect wiring of the Uninterruptable Power Supply, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIGNA Creator Recalled by GE Medical Systems, LLC Due to Possible incorrect...
The Issue: Possible incorrect wiring of the Uninterruptable Power Supply, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1.5T Signa HDx Recalled by GE Medical Systems, LLC Due to Possible incorrect...
The Issue: Possible incorrect wiring of the Uninterruptable Power Supply, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optima MR450 1.5T Product Usage: 1 .5T Brivo MR355 and Recalled by GE...
The Issue: Possible incorrect wiring of the Uninterruptable Power Supply, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Install CD Recalled by Medtronic Navigation, Inc. Due to Software issue...
The Issue: Software issue related to the StealthStation S7 system and the Synergy Spine...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vitality Spinal Fixation System Recalled by Zimmer Biomet Spine Inc. Due to...
The Issue: Zimmer Biomet is conducting a medical device recall for Vitality T27 Final...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1) ARROWg+ard Blue You-Blend Two-Lumen Hemodialysis Catheterization Kit for...
The Issue: Arrow International is recalling the affected product because the packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arterial Catheterization Kit Recalled by Arrow International Inc Due to...
The Issue: Arrow International is recalling the affected product because the packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cook Multi-Use Holmium Laser Fibers Recalled by Cook Inc. Due to Correction...
The Issue: Correction to the product Instructions for Use because the current...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1) ARROWg+ard Blue MAC Two-Lumen Central Venous Access Kit 2) Recalled by...
The Issue: Arrow International is recalling the affected product because the packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1) Pressure Injectable Multi-Lumen Central Venous Catheterization Kit 2)...
The Issue: Arrow International is recalling the affected product because the packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow Multi-Lumen CVC Kit The Arrow Two-Lumen Central Venous Access Recalled...
The Issue: The Arrow CVC is indicated to provide short-term (<30 days) central venous...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Multi-Lumen Central Venous Catheterization Kit with Blue FlexTip(R) Recalled...
The Issue: Arrow International is recalling the affected product because the packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Single-Lumen Central Venous Catheterization Kit with Blue FlexTip(R)...
The Issue: Arrow International is recalling the affected product because the packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow MAC Two-Lumen Central Venous Access Kit Introducer Catheter The...
The Issue: Arrow International is recalling the affected product because the packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARROWg+ard Blue CVC Kit The ARROWg+ard Blue CVCs are intended Recalled by...
The Issue: The Arrow CVC is indicated to provide short-term (<30 days) central venous...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.