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 9481–9500 of 27,850 recalls

Medical DeviceMay 12, 2021· Stryker Medical Division of Stryker Corporation

Recalled Item: ComfortGel - assists in the prevention and treatment of all Recalled by...

The Issue: Medical devices intended for use in a healthcare facility were distributed...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 12, 2021· Stryker Medical Division of Stryker Corporation

Recalled Item: Stretcher Chair-for use in all acute care hospitals and medical Recalled by...

The Issue: Medical devices intended for use in a healthcare facility were distributed...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 12, 2021· Stryker Medical Division of Stryker Corporation

Recalled Item: CUB Pediatric Crib- intended to provide a pediatric patient support Recalled...

The Issue: Medical devices intended for use in a healthcare facility were distributed...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 12, 2021· Stryker Medical Division of Stryker Corporation

Recalled Item: Transport Stretcher 747 - a non-powered Recalled by Stryker Medical Division...

The Issue: Medical devices intended for use in a healthcare facility were distributed...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 12, 2021· Stryker Medical Division of Stryker Corporation

Recalled Item: S3 MedSurg Bed - intended to support and transport patients Recalled by...

The Issue: Medical devices intended for use in a healthcare facility were distributed...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 12, 2021· Stryker Medical Division of Stryker Corporation

Recalled Item: InTouch 2131-intended to support a human patient in an acute care setting...

The Issue: Medical devices intended for use in a healthcare facility were distributed...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 12, 2021· Stryker Medical Division of Stryker Corporation

Recalled Item: Michael Graves with Stryker Highback Chair-intended for pediatric and adult...

The Issue: Medical devices intended for use in a healthcare facility were distributed...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 12, 2021· Stryker Medical Division of Stryker Corporation

Recalled Item: S3 MedSurg Bed - intended to support and transport patients Recalled by...

The Issue: Medical devices intended for use in a healthcare facility were distributed...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 12, 2021· Stryker Medical Division of Stryker Corporation

Recalled Item: Prime Big Wheel Stretcher-used as a short-term outpatient clinical...

The Issue: Medical devices intended for use in a healthcare facility were distributed...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 12, 2021· Stryker Medical Division of Stryker Corporation

Recalled Item: Prime Fifth Wheel Stretcher-stretcher may be used for minor procedures...

The Issue: Medical devices intended for use in a healthcare facility were distributed...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2021· Medical Action Industries, Inc. 306

Recalled Item: Medical Action INDUSTRIES INC. Recalled by Medical Action Industries, Inc....

The Issue: There is a potential for flaking metal and/or brown spots on the hemostats...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2021· Medical Action Industries, Inc. 306

Recalled Item: Medical Action INDUSTRIES INC. Recalled by Medical Action Industries, Inc....

The Issue: There is a potential for flaking metal and/or brown spots on the hemostats...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2021· Skytron, Div. The KMW Group, Inc

Recalled Item: Skyton Bracket Flatscreen Recalled by Skytron, Div. The KMW Group, Inc Due...

The Issue: Failure of the FS32 Monitor Brackets from the mounting block could...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2021· Medical Action Industries, Inc. 306

Recalled Item: Medical Action INDUSTRIES INC. Recalled by Medical Action Industries, Inc....

The Issue: There is a potential for flaking metal and/or brown spots on the hemostats...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2021· Medical Action Industries, Inc. 306

Recalled Item: Medical Action INDUSTRIES INC. Recalled by Medical Action Industries, Inc....

The Issue: There is a potential for flaking metal and/or brown spots on the hemostats...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2021· Exactech, Inc.

Recalled Item: Humeral Augmented Tray (HAT) trials that are components of KIT-321HAT....

The Issue: The HAT trial contains a retaining ring that has shown the potential to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2021· Medical Action Industries, Inc. 306

Recalled Item: novaplus Recalled by Medical Action Industries, Inc. 306 Due to There is a...

The Issue: There is a potential for flaking metal and/or brown spots on the hemostats...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2021· IMPLANTCAST GMBH

Recalled Item: EcoFit cup cementless: Model(Catalog Number)/Description: 02200046 /EcoFit...

The Issue: A risk exists during impacting of the acetabular cup into the bone the plugs...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2021· BioFire Diagnostics, LLC

Recalled Item: BioFire BCID2 Panel Recalled by BioFire Diagnostics, LLC Due to Elevated...

The Issue: Elevated rates of false negative results may occur when using blood culture...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2021· Randox Laboratories Ltd.

Recalled Item: NEFA CAL (Non-Esterified Fatty Acids)- IVD Standard for measurement of...

The Issue: Standard packed within NEFA kit has been assigned incorrectly. Calibrating...

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

Class II — Potential Health HazardOngoing