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. 2,062 recalls have been distributed to New Mexico in the last 12 months.

48,595 total recalls
2,062 in last 12 months

Showing 33813400 of 48,595 recalls

Medical DeviceDecember 23, 2024· Percussionaire Corporation

Recalled Item: VDR4 Phasitron Breathing Circuit Models that contain the venturi component:...

The Issue: Due to internal venturi component getting transiently stuck in the forward...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 23, 2024· Hollister Incorporated

Recalled Item: AnchorFast Guard Recalled by Hollister Incorporated Due to Hollister...

The Issue: Hollister received reports of decreased skin barrier wear time which could...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2024· Accuray Incorporated

Recalled Item: CyberKnife Treatment Delivery System Recalled by Accuray Incorporated Due to...

The Issue: Snap rings may become partially or completed detached from the shafts within...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2024· Hollister Incorporated

Recalled Item: AnchorFast Recalled by Hollister Incorporated Due to Hollister received...

The Issue: Hollister received reports of decreased skin barrier wear time which could...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2024· Hollister Incorporated

Recalled Item: AnchorFast Guard Select Recalled by Hollister Incorporated Due to Hollister...

The Issue: Hollister received reports of decreased skin barrier wear time which could...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2024· Hollister Incorporated

Recalled Item: AnchorFast SlimFit Recalled by Hollister Incorporated Due to Hollister...

The Issue: Hollister received reports of decreased skin barrier wear time which could...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2024· Boston Scientific Corporation

Recalled Item: AXIOS Stent and Electrocautery- Enhanced Delivery System 15mmx15mm UPN:...

The Issue: Reported Outer sheath distal black tip detaching from the device can remain...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2024· Ethicon, LLC

Recalled Item: ETHIBOND EXCEL Polyester Suture Recalled by Ethicon, LLC Due to Sutures may...

The Issue: Sutures may have an open seal on the primary packaging, due to a...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2024· Randox Laboratories, Limited

Recalled Item: Randox Lipoprotein (a) - In vitro diagnostic (IVD) use as Recalled by Randox...

The Issue: Lipoprotein (a) on Roche Cobas c501 with nmol/l claims does not have a...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2024· Baxter Healthcare Corporation

Recalled Item: Baxter Continu-Flo Solution Set with Duo-Vent Spike Recalled by Baxter...

The Issue: Specific lots of Solution Sets with Duo-Vent Spike have the potential for...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2024· Ethicon, LLC

Recalled Item: PERMA-HAND Silk Suture Recalled by Ethicon, LLC Due to Sutures may have an...

The Issue: Sutures may have an open seal on the primary packaging, due to a...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2024· Baxter Healthcare Corporation

Recalled Item: Welch Allyn Recalled by Baxter Healthcare Corporation Due to There is an...

The Issue: There is an issue with the ventilator battery charger that could lead to an...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 20, 2024· Boston Scientific Corporation

Recalled Item: AXIOS Stent and Electrocautery- Enhanced Delivery System 20mmx10mm UPN:...

The Issue: Reported Outer sheath distal black tip detaching from the device can remain...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2024· Baxter Healthcare Corporation

Recalled Item: Welch Allyn Recalled by Baxter Healthcare Corporation Due to There is an...

The Issue: There is an issue with the ventilator battery charger that could lead to an...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 20, 2024· Boston Scientific Corporation

Recalled Item: AXIOS Stent and Electrocautery- Enhanced Delivery System 15mmx10mm UPN:...

The Issue: Reported Outer sheath distal black tip detaching from the device can remain...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2024· Randox Laboratories, Limited

Recalled Item: Randox Lipoprotein (a) - In vitro diagnostic (IVD) use as Recalled by Randox...

The Issue: Lipoprotein (a) on Roche Cobas c501 with nmol/l claims does not have a...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2024· Boston Scientific Corporation

Recalled Item: HOT AXIOS Stent and Electrocautery- Enhanced Delivery System 15mmx10mm UPN:...

The Issue: Reported Outer sheath distal black tip detaching from the device can remain...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2024· Baxter Healthcare Corporation

Recalled Item: Breathe Technologies Recalled by Baxter Healthcare Corporation Due to There...

The Issue: There is an issue with the ventilator battery charger that could lead to an...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 20, 2024· Baxter Healthcare Corporation

Recalled Item: Baxter Solution Set with Duo-Vent Spike Recalled by Baxter Healthcare...

The Issue: Specific lots of Solution Sets with Duo-Vent Spike have the potential for...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2024· Boston Scientific Corporation

Recalled Item: AXIOS Stent and Electrocautery- Enhanced Delivery System 8mmx8mm UPN:...

The Issue: Reported Outer sheath distal black tip detaching from the device can remain...

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

Class II — Potential Health HazardOngoing