Product Recalls in Tennessee

Product recalls affecting Tennessee — including food, drugs, consumer products, medical devices, and vehicles distributed to Tennessee. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,645 recalls have been distributed to Tennessee in the last 12 months.

52,000 total recalls
2,645 in last 12 months

Showing 1082110840 of 52,000 recalls

Medical DeviceDecember 7, 2022· Mobius Imaging, LLC

Recalled Item: MobiCT-32 AIRO Mobile CT Scanner Recalled by Mobius Imaging, LLC Due to...

The Issue: Stryker received one report of an injury to an untrained user that occurred...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2022· Johnson & Johnson Surgical Vision, Inc.

Recalled Item: Veritas Advanced Infusion Packs Recalled by Johnson & Johnson Surgical...

The Issue: Weld protrusion/physical gap between the housing and phaco pack cover, may...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2022· The Anspach Effort, Inc.

Recalled Item: Pediatric Craniotome Recalled by The Anspach Effort, Inc. Due to Ball...

The Issue: Ball bearings in the CRANI-A (ANSPACH Power Tools Adult Craniotome...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2022· The Anspach Effort, Inc.

Recalled Item: 6.5 cm Pediatric Craniotome Attachment. Use with XMax¿ Recalled by The...

The Issue: Ball bearings in the CRANI-A (ANSPACH Power Tools Adult Craniotome...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Surgical convenience kits labeled as: a) MEDLINE HAND PACK Recalled by...

The Issue: The recall is due to the perforated bag not allowing for outside of the kit...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Surgical convenience kits labeled as: a) MEDLINE GENERAL UTILITY Recalled by...

The Issue: The recall is due to the perforated bag not allowing for outside of the kit...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Surgical convenience kits labeled as: MEDLINE PREP TRAY Recalled by MEDLINE...

The Issue: The recall is due to the perforated bag not allowing for outside of the kit...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Surgical convenience kits labeled as: a) CENTURION MEDICAL PRODUCTS CENTRAL...

The Issue: The recall is due to the perforated bag not allowing for outside of the kit...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Surgical convenience kits labeled as: CENTURION MEDICAL PRODUCTS NEONATAL...

The Issue: The recall is due to the perforated bag not allowing for outside of the kit...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2022· Philips Respironics, Inc.

Recalled Item: Philips Garbin Ventilator Recalled by Philips Respironics, Inc. Due to The...

The Issue: The replacement silicone sound abatement foam installed into some Trilogy...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 7, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Surgical convenience kits labeled as: MEDLINE CABG PACK Recalled by MEDLINE...

The Issue: The recall is due to the perforated bag not allowing for outside of the kit...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Surgical convenience kits labeled as: CENTURION MEDICAL PRODUCTS IR...

The Issue: The recall is due to the perforated bag not allowing for outside of the kit...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2022· The Anspach Effort, Inc.

Recalled Item: 6.5 cm Adult Rotating Craniotome Attachment. Use with XMax¿ Recalled by The...

The Issue: Ball bearings in the CRANI-A (ANSPACH Power Tools Adult Craniotome...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Surgical convenience kits labeled as: MEDLINE ANGIO PORT KIT W/HIGH GRADE IN...

The Issue: The recall is due to the perforated bag not allowing for outside of the kit...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2022· The Anspach Effort, Inc.

Recalled Item: 6.5 cm Adult Craniotome Recalled by The Anspach Effort, Inc. Due to Ball...

The Issue: Ball bearings in the CRANI-A (ANSPACH Power Tools Adult Craniotome...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2022· The Anspach Effort, Inc.

Recalled Item: 6.5 cm Adult Rotating Craniotome Attachment. Use with XMax¿ Recalled by The...

The Issue: Ball bearings in the CRANI-A (ANSPACH Power Tools Adult Craniotome...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2022· Philips Respironics, Inc.

Recalled Item: Philips Trilogy 200 Ventilator Recalled by Philips Respironics, Inc. Due to...

The Issue: The replacement silicone sound abatement foam installed into some Trilogy...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 7, 2022· The Anspach Effort, Inc.

Recalled Item: 7.5 cm Large Craniotome Attachment Use with XMax¿ Recalled by The Anspach...

The Issue: Ball bearings in the CRANI-A (ANSPACH Power Tools Adult Craniotome...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Surgical convenience kits labeled as: CENTURION MEDICAL PRODUCTS...

The Issue: The recall is due to the perforated bag not allowing for outside of the kit...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Surgical convenience kits labeled as: MEDLINE ARM/MINOR DRAPE CSTM Recalled...

The Issue: The recall is due to the perforated bag not allowing for outside of the kit...

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

Class II — Potential Health HazardOngoing