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.

48,595 total recalls
2,605 in last 12 months

Showing 19812000 of 27,850 recalls

Medical DeviceFebruary 25, 2025· Stryker Corporation

Recalled Item: Hemopore 8cm nasal/sinus temporary wound dressing Recalled by Stryker...

The Issue: There is a potential for blister seals on the product to present a bubble on...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2025· Stryker Corporation

Recalled Item: Hemopore 2PK nasal/sinus temporary wound dressing Recalled by Stryker...

The Issue: There is a potential for blister seals on the product to present a bubble on...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2025· Stryker Corporation

Recalled Item: Nasopore Standard 8cm fragmentable nasal dressing Recalled by Stryker...

The Issue: There is a potential for blister seals on the product to present a bubble on...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2025· Stryker Corporation

Recalled Item: Nasopore 4cm Standard 2PK fragmentable nasal dressing Recalled by Stryker...

The Issue: There is a potential for blister seals on the product to present a bubble on...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2025· Stryker Corporation

Recalled Item: Nasopore 8cm fragmentable nasal dressing Recalled by Stryker Corporation Due...

The Issue: There is a potential for blister seals on the product to present a bubble on...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2025· Stryker Corporation

Recalled Item: Nasopore Standard 4cm fragmentable nasal dressing Recalled by Stryker...

The Issue: There is a potential for blister seals on the product to present a bubble on...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2025· Stryker Corporation

Recalled Item: Nasopore Ex Firm 4cm fragmentable nasal dressing Recalled by Stryker...

The Issue: There is a potential for blister seals on the product to present a bubble on...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2025· Stryker Corporation

Recalled Item: Nasopore Ex Firm 8cm fragmentable nasal dressing Recalled by Stryker...

The Issue: There is a potential for blister seals on the product to present a bubble on...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2025· Stryker Corporation

Recalled Item: Nasopore 4cm fragmentable nasal dressing Recalled by Stryker Corporation Due...

The Issue: There is a potential for blister seals on the product to present a bubble on...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2025· Stryker Corporation

Recalled Item: Otopore Cylinder Standard outer ear dressings Recalled by Stryker...

The Issue: There is a potential for blister seals on the product to present a bubble on...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2025· Stryker Corporation

Recalled Item: Nasopore 4cm Standard 2PK fragmentable nasal dressing Recalled by Stryker...

The Issue: There is a potential for blister seals on the product to present a bubble on...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2025· Baxter Healthcare Corporation

Recalled Item: Baxter TruSystem 7500 Recalled by Baxter Healthcare Corporation Due to There...

The Issue: There is a software issue which causes the upper back section to not be...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2025· Baxter Healthcare Corporation

Recalled Item: Baxter TruSystem 7500 Hybrid Plus (FC) Recalled by Baxter Healthcare...

The Issue: There is a software issue which causes the upper back section to not be...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2025· Baxter Healthcare Corporation

Recalled Item: Baxter Mobile column TruSystem 7500 U Recalled by Baxter Healthcare...

The Issue: There is a software issue which causes the upper back section to not be...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2025· Baxter Healthcare Corporation

Recalled Item: Baxter Stationary column TruSystem 7500 Recalled by Baxter Healthcare...

The Issue: There is a software issue which causes the upper back section to not be...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2025· Baxter Healthcare Corporation

Recalled Item: Baxter TruSystem 7500 Hybrid (MC) Recalled by Baxter Healthcare Corporation...

The Issue: There is a software issue which causes the upper back section to not be...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2025· Baxter Healthcare Corporation

Recalled Item: Baxter TruSystem 7500 Hybrid (SC) Recalled by Baxter Healthcare Corporation...

The Issue: There is a software issue which causes the upper back section to not be...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2025· Baxter Healthcare Corporation

Recalled Item: Baxter Stationary column TruSystem 7500 U Recalled by Baxter Healthcare...

The Issue: There is a software issue which causes the upper back section to not be...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2025· Baxter Healthcare Corporation

Recalled Item: Baxter TruSystem 7500 Hybrid MR IMRIS Recalled by Baxter Healthcare...

The Issue: There is a software issue which causes the upper back section to not be...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2025· Baxter Healthcare Corporation

Recalled Item: Baxter Operating table column TS7500 MOBIUS Recalled by Baxter Healthcare...

The Issue: There is a software issue which causes the upper back section to not be...

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

Class II — Potential Health HazardOngoing