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. 2,670 recalls have been distributed to Tennessee in the last 12 months.

52,000 total recalls
2,670 in last 12 months

Showing 76017620 of 29,188 recalls

Medical DeviceSeptember 30, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: BAUSCH + LOMB BASIC OPHTHALMIC PACK Recalled by MEDLINE INDUSTRIES, LP -...

The Issue: Medline received complaints on some of the breather pouches with in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 30, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: BAUSCH + LOMB CATARACT TRAY Recalled by MEDLINE INDUSTRIES, LP - Northfield...

The Issue: Medline received complaints on some of the breather pouches with in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 30, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE LITHOTOMY Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to...

The Issue: Medline received complaints on some of the breather pouches with in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 30, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: BAUSCH + LOMB PHACO PACK Recalled by MEDLINE INDUSTRIES, LP - Northfield Due...

The Issue: Medline received complaints on some of the breather pouches with in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 30, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: BAUSCH + LOMB EYE PACK Recalled by MEDLINE INDUSTRIES, LP - Northfield Due...

The Issue: Medline received complaints on some of the breather pouches with in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 30, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: BAUSCH + LOMB CATARACT PACK Recalled by MEDLINE INDUSTRIES, LP - Northfield...

The Issue: Medline received complaints on some of the breather pouches with in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 30, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE LINQ TRAY Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to...

The Issue: Medline received complaints on some of the breather pouches with in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 30, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: BAUSCH + LOMB CATARACT PACK Recalled by MEDLINE INDUSTRIES, LP - Northfield...

The Issue: Medline received complaints on some of the breather pouches with in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 30, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: BAUSCH + LOMB EYE MUSCLE Recalled by MEDLINE INDUSTRIES, LP - Northfield Due...

The Issue: Medline received complaints on some of the breather pouches with in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 30, 2022· Wright Medical Technology, Inc.

Recalled Item: Stryker INBONE Tibial Tray Recalled by Wright Medical Technology, Inc. Due...

The Issue: The tibial tray lock detail is oversized (larger than specification).

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 30, 2022· Wright Medical Technology, Inc.

Recalled Item: Stryker INBONE Tibial Tray Recalled by Wright Medical Technology, Inc. Due...

The Issue: The tibial tray lock detail is oversized (larger than specification).

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 29, 2022· Canon Medical System, USA, INC.

Recalled Item: Canon Aplio ultrasound system Recalled by Canon Medical System, USA, INC....

The Issue: After completion, ultrasound system's Stress Echo may not terminate if user...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2022· Biokit, S.A.

Recalled Item: biokitHSV-2 Rapid Test Recalled by Biokit, S.A. Due to HSV-2 rapid test may...

The Issue: HSV-2 rapid test may report false positive results.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2022· TELEFLEX LLC

Recalled Item: Pilling Wecksorb Cylindrical Sponges Recalled by TELEFLEX LLC Due to...

The Issue: Specific lots have not been irradiated to eliminate pyronema and therefore...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2022· Kamiya Biomedical Company, LLC

Recalled Item: K-ASSAY IgA Immunoturbidimetric Assay Recalled by Kamiya Biomedical Company,...

The Issue: IgA Reagent may start showing cloudiness over time, which can affect assay...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2022· Covidien, LP

Recalled Item: Endo Stitch V-Loc 180 Absorbable Reload Recalled by Covidien, LP Due to...

The Issue: Medtronic has received 210 reports of needles breaking during endoscopic...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2022· Covidien, LP

Recalled Item: Endo Stitch V-Loc PBT Non-Absorbable Reload Recalled by Covidien, LP Due to...

The Issue: Medtronic has received 210 reports of needles breaking during endoscopic...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2022· Cardinal Health 200, LLC

Recalled Item: Cardinal Health GEL PACK REUSABLE Recalled by Cardinal Health 200, LLC Due...

The Issue: Users are being informed that the product should not be used on...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2022· Cardinal Health 200, LLC

Recalled Item: Cardinal Health INSULATED GEL PACK REUSABLE Recalled by Cardinal Health 200,...

The Issue: Users are being informed that the product should not be used on...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2022· Cardinal Health 200, LLC

Recalled Item: Cardinal Health Reusable Gel Pack Recalled by Cardinal Health 200, LLC Due...

The Issue: Users are being informed that the product should not be used on...

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

Class II — Potential Health HazardOngoing