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. 2,605 recalls have been distributed to New Mexico in the last 12 months.
Showing 2181–2200 of 48,595 recalls
Recalled Item: Peak Cocktails Blood Orange Spritz 8.4 fl oz aluminum cans Recalled by Peak...
The Issue: Overpressurization leading to exploding cans
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Hamilton C6 (ESM Board PN 10144626 UDI-DI code: Recalled by Hamilton Medical...
The Issue: A mechanical defect on a printed circuit board (PCB) as a result of PCB...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SwabCap Disinfecting Cap for Needlefree Connectors: SwabSleeve Recalled by...
The Issue: Due to a manufacturing issue, disinfecting cap for needle-free connectors...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bravo CF capsule delivery device Recalled by Given Imaging Ltd. Due to It...
The Issue: It has been determined that misapplied adhesive on the Bravo CF capsule...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by C.R. Bard Inc Due to Cather packaging may contain the incorrect...
The Issue: Cather packaging may contain the incorrect French size.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Heyman Follower Straight Tip for following sizes: 10Fr - Recalled by C.R....
The Issue: Cather packaging may contain the incorrect French size.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Heyman Follower Coude Tip for following sizes: 12Fr - Recalled by C.R....
The Issue: Cather packaging may contain the incorrect French size.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KETAmine Hydrochloride Injection Recalled by Tailstorm Health INC Due to...
The Issue: Lack of Assurance of Sterility: A recent FDA inspection revealed concerns...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: LIDOcaine HCL Sterile Injection Recalled by Tailstorm Health INC Due to Lack...
The Issue: Lack of Assurance of Sterility: A recent FDA inspection revealed concerns...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: KETAmine Hydrochloride Injection Recalled by Tailstorm Health INC Due to...
The Issue: Lack of Assurance of Sterility: A recent FDA inspection revealed concerns...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BUPIVAcaine HCL Sterile injection Recalled by Tailstorm Health INC Due to...
The Issue: Lack of Assurance of Sterility: A recent FDA inspection revealed concerns...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: LIDOcaine HCl Injection Recalled by Tailstorm Health INC Due to Lack of...
The Issue: Lack of Assurance of Sterility: A recent FDA inspection revealed concerns...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: LIDOcaine HCL Sterile Injection Recalled by Tailstorm Health INC Due to Lack...
The Issue: Lack of Assurance of Sterility: A recent FDA inspection revealed concerns...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sulfamethoxazole and Trimethoprim Tablets Recalled by Amneal...
The Issue: Microbial contamination of non-sterile products: tablets may exhibit black...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Medshape Universal Joints Recalled by Medshape, INC. Due to Bone external...
The Issue: Bone external fixation system may have the pin that can become dislodged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Platelia Toxo IgM Catalog Number 26211 UDI Code: 03610520005552 The Recalled...
The Issue: Due to a risk of false positive results that could lead to unnecessary...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Inseego USB8 4G Dongle Kit Recalled by Remote Diagnostic Technologies Ltd....
The Issue: Kit USB flash drive contains outdated software, which could result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Servo-u Ventilator System. Model Number: 6688600. Recalled by Maquet...
The Issue: Potential for inaccurate measurement of the patient circuit compliance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Servo-n Ventilator System. Model Number: 6694800. Recalled by Maquet...
The Issue: Potential for inaccurate measurement of the patient circuit compliance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Servo-u MR Ventilator System. Model Number: 6888800. Recalled by Maquet...
The Issue: Potential for inaccurate measurement of the patient circuit compliance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.