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. 1,090 recalls have been distributed to New Mexico in the last 12 months.
Showing 3741–3760 of 27,850 recalls
Recalled Item: Soltive SuperPulsed Laser System Wireless Footswitch Recalled by Olympus...
The Issue: Difficulties in pairing the wireless footswitch with the Soltive Laser,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The VASOVIEW HEMOPRO Endoscopic Vessel Harvesting Systems is designed for...
The Issue: There were 27 complaints between March 22, 2024, and April 30, 2024, related...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AXIOM MULTIX MP - Inended Radiographic X ray Table is Recalled by Siemens...
The Issue: Short circuit in the power supply unit (PSU) of the Touch Display may lead...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MIC-KEY* Gastric-Jejunal Feeding Tube Kit Recalled by Avanos Medical, Inc....
The Issue: The IFU was missing some risk information requested by another country to be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Volara System. Blue Ventilator Adapter Module. Intermittent positive...
The Issue: Potential of the handset plug to disconnect from the nebulizer port on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Titan Blis-Sonic Scaler packaged with the Titan Scaler Tip - Recalled by...
The Issue: Tip holder portion of the scaler tip assembly may have an oversized...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Titan Scaler Tip - Perio Model/Catalog Number: 261669 The scaler Recalled by...
The Issue: Tip holder portion of the scaler tip assembly may have an oversized...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Volara System. Single Patient Use (SPU) Circuit 5kit for Volara Recalled by...
The Issue: Potential of the handset plug to disconnect from the nebulizer port on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Life2000 Ventilator Recalled by Baxter Healthcare Corporation Due to...
The Issue: Potential for certain Life2000 ventilator systems to either fail to charge...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Presource kits and trays Recalled by Cardinal Health 200, LLC Due to...
The Issue: Cardinal Health is following the FDA's recommendations regarding the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Presource kits and trays Recalled by Cardinal Health 200, LLC Due to...
The Issue: Cardinal Health is following the FDA's recommendations regarding the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Presource kits and trays Recalled by Cardinal Health 200, LLC Due to...
The Issue: Cardinal Health is following the FDA's recommendations regarding the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Presource kits and trays Recalled by Cardinal Health 200, LLC Due to...
The Issue: Cardinal Health is following the FDA's recommendations regarding the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CUSA Excel C2600 23KHz Straight Handpiece-Indicated for use in surgical...
The Issue: Potential for the CUSA Excel 23KHz Straight Handpiece housing to crack, may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (1) CryoPatch SG Pulmonary Human Cardiac Hemi-Artery - Artery Patch Recalled...
The Issue: Grafts were found to have been approved, released, shipped and implanted...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CryoValve SG Pulmonary Human Heart Valve Recalled by Artivion, Inc Due to...
The Issue: Grafts were found to have been approved, released, shipped and implanted...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: PROBEAT Product Name: PROBEAT-FR Model/Catalog Number: N/A...
The Issue: During positioning within the system's 3D to 3D matching mode while...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: PROBEAT Product Name: PROBEAT-CR Model/Catalog Number: N/A...
The Issue: During positioning within the system's 3D to 3D matching mode while...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: PROBEAT Product Name: PROBEAT-V Model/Catalog Number: N/A...
The Issue: During positioning within the system's 3D to 3D matching mode while...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Beckman Coulter Recalled by Beckman Coulter Inc. Due to LIH Influence check...
The Issue: LIH Influence check settings for Lipemia are incorrect which may result...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.