Product Recalls in South Dakota

Product recalls affecting South Dakota — including food, drugs, consumer products, medical devices, and vehicles distributed to South Dakota. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,060 recalls have been distributed to South Dakota in the last 12 months.

47,632 total recalls
1,060 in last 12 months

Showing 7461–7480 of 27,558 recalls

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: CENTURION MEDICAL PRODUCTS NICU PICC INSERTION BUNDLE W/O Recalled by...

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· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE DENTAL PACK 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· Boston Scientific Corporation

Recalled Item: EMBLEM S-ICD Recalled by Boston Scientific Corporation Due to There is an...

The Issue: There is an incorrect manufacturing date/timestamp within the software which...

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 CVC BARRIER KIT 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 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· 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
Medical DeviceSeptember 28, 2022· X-NAV Technologies, LLC

Recalled Item: X-Guide X-Mark Probe Tool -used for registering edentulous patients to...

The Issue: Product missing one of two welds connecting the tip to the shaft, if the...

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 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 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 HOT AND COLD GEL PACK REUSABLE Recalled by Cardinal Health...

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