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. 1,006 recalls have been distributed to New Mexico in the last 12 months.

48,595 total recalls
1,006 in last 12 months

Showing 18121–18140 of 48,595 recalls

Medical DeviceApril 24, 2020· LivaNova USA Inc.

Recalled Item: Sterile Disposable Connectors ASY Y CONN 3/8 X 3/8 X Recalled by LivaNova...

The Issue: The firm has identified through internal tests that the sterile barrier of...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2020· LivaNova USA Inc.

Recalled Item: 3/8X3/8X3/8 Y CONN Recalled by LivaNova USA Inc. Due to XXX

The Issue: XXX

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2020· LivaNova USA Inc.

Recalled Item: Sterile Disposable Connectors ASY STR CONN 1/4 STRLE 24. REF/ Recalled by...

The Issue: The firm has identified through internal tests that the sterile barrier of...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2020· LivaNova USA Inc.

Recalled Item: Sterile Disposable Connectors ASY RDC Y 1/2X3/8X3/8 STR 24 REF/ Recalled by...

The Issue: The firm has identified through internal tests that the sterile barrier of...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2020· LivaNova USA Inc.

Recalled Item: Sterile Disposable Connectors ASY S CONN 3/16X1/8 RDR ANLD24 REF/ Recalled...

The Issue: The firm has identified through internal tests that the sterile barrier of...

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

Class II — Potential Health HazardOngoing
DrugApril 24, 2020· Dr. Reddy's Laboratories, Inc.

Recalled Item: Esomeprazole Magnesium Delayed Release Capsules USP Recalled by Dr. Reddy's...

The Issue: Discoloration: product contains brown pellets

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

Class III — Low RiskOngoing
Refund
DrugApril 23, 2020· QuVa Pharma, Inc.

Recalled Item: R.E.C.K. (Ropivacaine Recalled by QuVa Pharma, Inc. Due to Presence of...

The Issue: Presence of Particulate Matter: Fresenius Kabi recalling vials of Ketorolac

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

Class III — Low RiskOngoing
Refund
Medical DeviceApril 23, 2020· Access Scientific LLC

Recalled Item: BD PosiFlush SF Saline Flush Syringe 10 mL used in Recalled by Access...

The Issue: Saline Flush Syringe compromised sterility due to holes in the packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2020· Philips North America, LLC

Recalled Item: ProxiDiagnost N90 Recalled by Philips North America, LLC Due to The thermo...

The Issue: The thermo switches in the three-phase transformer, which normally aid in...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2020· Access Scientific LLC

Recalled Item: BD PosiFlush SF Saline Flush Syringe 10 mL used in Recalled by Access...

The Issue: Saline Flush Syringe compromised sterility due to holes in the packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2020· Olympus Corporation of the Americas

Recalled Item: OLYMPUS ShockPulse-SE Lithotripsy System Recalled by Olympus Corporation of...

The Issue: A component of the Olympus ShockPulse Transducer was manufactured with...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2020· Access Scientific LLC

Recalled Item: BD PosiFlush SF Saline Flush Syringe 10 mL used in Recalled by Access...

The Issue: Saline Flush Syringe compromised sterility due to holes in the packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2020· Access Scientific LLC

Recalled Item: BD PosiFlush SF Saline Flush Syringe 10 mL used in Recalled by Access...

The Issue: Saline Flush Syringe compromised sterility due to holes in the packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2020· Access Scientific LLC

Recalled Item: BD PosiFlush SF Saline Flush Syringe 10 mL used in Recalled by Access...

The Issue: Saline Flush Syringe compromised sterility due to holes in the packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2020· Access Scientific LLC

Recalled Item: BD PosiFlush SF Saline Flush Syringe 10 mL used in Recalled by Access...

The Issue: Saline Flush Syringe compromised sterility due to holes in the packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2020· Access Scientific LLC

Recalled Item: BD PosiFlush SF Saline Flush Syringe 10 mL used in Recalled by Access...

The Issue: Saline Flush Syringe compromised sterility due to holes in the packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2020· Access Scientific LLC

Recalled Item: BD PosiFlush SF Saline Flush Syringe 10 mL used in Recalled by Access...

The Issue: Saline Flush Syringe compromised sterility due to holes in the packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2020· Access Scientific LLC

Recalled Item: BD PosiFlush SF Saline Flush Syringe 10 mL used in Recalled by Access...

The Issue: Saline Flush Syringe compromised sterility due to holes in the packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2020· Access Scientific LLC

Recalled Item: BD PosiFlush SF Saline Flush Syringe 10 mL used in Recalled by Access...

The Issue: Saline Flush Syringe compromised sterility due to holes in the packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2020· Access Scientific LLC

Recalled Item: BD PosiFlush SF Saline Flush Syringe 10 mL used in Recalled by Access...

The Issue: Saline Flush Syringe compromised sterility due to holes in the packaging.

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

Class II — Potential Health HazardOngoing