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. 1,078 recalls have been distributed to New Mexico in the last 12 months.

48,595 total recalls
1,078 in last 12 months

Showing 8761–8780 of 27,850 recalls

Medical DeviceOctober 21, 2021· Philips North America Llc

Recalled Item: CombiDiagnost R90 1.0 and 1.1 multi-functional general R/F system Recalled...

The Issue: If the system experiences an overvoltage / power surge it can cause a short...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2021· Boston Scientific Corporation

Recalled Item: HURRICANE RX DILATION BALLOON 6MM 4CM- -for endoscopic dilatation of...

The Issue: Balloon pinhole results in losss pressure or fails to gain or maintain...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2021· Boston Scientific Corporation

Recalled Item: HURRICANE RX DILATION BALLOON 4MM 4CM-for endoscopic dilatation of...

The Issue: Balloon pinhole results in losss pressure or fails to gain or maintain...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2021· Boston Scientific Corporation

Recalled Item: HURRICANE RX DILATION BALLOON 4MM 2CM-for endoscopic dilatation of...

The Issue: Balloon pinhole results in losss pressure or fails to gain or maintain...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2021· Philips North America Llc

Recalled Item: ProxiDiagnost R90 1.0 and 1.1 multi-functional general R/F system Recalled...

The Issue: If the system experiences an overvoltage / power surge it can cause a short...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2021· Siemens Medical Solutions USA, Inc

Recalled Item: Artis Q.zen ceiling with software VD12-angiography systems developed for...

The Issue: If SID (source-to-image distance) lift movement is activated and x-ray shall...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2021· Siemens Medical Solutions USA, Inc

Recalled Item: Artis Q biplane with software VD12-angiography systems developed for single...

The Issue: If SID (source-to-image distance) lift movement is activated and x-ray shall...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2021· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zee floor with software VD12-angiography systems developed for single...

The Issue: If SID (source-to-image distance) lift movement is activated and x-ray shall...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2021· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zee ceiling with software VD12-angiography systems developed for...

The Issue: If SID (source-to-image distance) lift movement is activated and x-ray shall...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2021· Siemens Medical Solutions USA, Inc

Recalled Item: Artis Q ceiling with software VD12-angiography systems developed for single...

The Issue: If SID (source-to-image distance) lift movement is activated and x-ray shall...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2021· Siemens Medical Solutions USA, Inc

Recalled Item: Artis Q.zen biplane with software VD12- angiography systems developed for...

The Issue: If SID (source-to-image distance) lift movement is activated and x-ray shall...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2021· MICROVENTION INC.

Recalled Item: Aspiration Syringe Kit Recalled by MICROVENTION INC. Due to Syringe Kits...

The Issue: Syringe Kits labeled for distribution OUS were inadvertently shipped to US...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2021· Siemens Medical Solutions USA, Inc

Recalled Item: Artis Q floor with software VD12- angiography systems developed for Recalled...

The Issue: If SID (source-to-image distance) lift movement is activated and x-ray shall...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2021· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zee multi-purpose with software VD12-angiography systems developed for...

The Issue: If SID (source-to-image distance) lift movement is activated and x-ray shall...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2021· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zee biplane with software VD12-angiography systems developed for...

The Issue: If SID (source-to-image distance) lift movement is activated and x-ray shall...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2021· Siemens Medical Solutions USA, Inc

Recalled Item: Artis Q.zen floor with software VD12-angiography systems developed for...

The Issue: If SID (source-to-image distance) lift movement is activated and x-ray shall...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2021· Medtronic Neuromodulation

Recalled Item: Model B35200 - Percept PC BrainSense Implantable Neurostimulator Recalled by...

The Issue: During cardioversion events, the Model B35200 Percept PC Implantable...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2021· InfuTronix LLC

Recalled Item: Nimbus PainPro Ambulatory Infusion Pumps with software version v4 Recalled...

The Issue: An unreleased Version 4 Protocol Library was installed on Nimbus PainPro (H)...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 18, 2021· Roche Diagnostics Operations, Inc.

Recalled Item: Cobas u 601 urinalysis test system Recalled by Roche Diagnostics Operations,...

The Issue: A potential risk for false negative nitrite results exists when endogenous...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 15, 2021· GE Healthcare, LLC

Recalled Item: GE Centricity Universal Viewer Zero Footprint Client Recalled by GE...

The Issue: There is a potential to display incomplete patient imaging study.

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

Class II — Potential Health HazardOngoing