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. 2,516 recalls have been distributed to South Dakota in the last 12 months.

47,632 total recalls
2,516 in last 12 months

Showing 74417460 of 27,558 recalls

Medical DeviceOctober 10, 2022· Caire, Inc.

Recalled Item: CAIRE Liberator 45 Recalled by Caire, Inc. Due to An audit discovered some...

The Issue: An audit discovered some inconsistencies in weld penetration on the...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 10, 2022· Hologic, Inc

Recalled Item: Hologic Sizer Set- sterilization tray and 6 individual sizers Recalled by...

The Issue: IFU was not provided with the Sizer Set sterilization tray Revised...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 7, 2022· Ferno-Washington Inc

Recalled Item: FERNO POWER X1 AMBULANCE COT- Item #0015807/UDI-DI 00190790002183 with 36V...

The Issue: Batteries could become unstable when not properly maintained and/or...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2022· Edwards Lifesciences, LLC

Recalled Item: Fogarty Biliary Balloon Probes Model Number: 410235FP 410405FP 410236FP...

The Issue: Due to an increase of confirmed latex deterioration complaints for arterial...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2022· Edwards Lifesciences, LLC

Recalled Item: Fogarty Arterial Embolectomy Catheters Model Number: 120602FP 120403FP...

The Issue: Due to an increase of confirmed latex deterioration complaints for arterial...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2022· Fresenius Medical Care Holdings, Inc.

Recalled Item: NaturaLyte Liquid Acid concentrate Recalled by Fresenius Medical Care...

The Issue: The "Nominal Chemical Composition" section of the label incorrectly lists...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 3, 2022· Becton, Dickinson and Company, BD Biosciences

Recalled Item: BD Trucount Tubes (Cat. No. 663028) Recalled by Becton, Dickinson and...

The Issue: Due to partial label detachment on tubes. This can cause tubes to become...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 3, 2022· Becton, Dickinson and Company, BD Biosciences

Recalled Item: BD Multitest 6-Color TBNK with optional BD Trucount Tubes (Cat. No. 662995)...

The Issue: Due to partial label detachment on tubes. This can cause tubes to become...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 3, 2022· Rebiscan, Inc.

Recalled Item: Blinq Pediatric Vision Scanner-Pediatric Vision Scanner-intended for...

The Issue: Unable to charge the battery pack- battery packs will allow the batteries to...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 3, 2022· Becton, Dickinson and Company, BD Biosciences

Recalled Item: BD Trucount Tubes (Cat. No. 340334) Recalled by Becton, Dickinson and...

The Issue: Due to partial label detachment on tubes. This can cause tubes to become...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 3, 2022· Beckman Coulter, Inc.

Recalled Item: MicroScan autoSCAN-4 Instrument Recalled by Beckman Coulter, Inc. Due to Due...

The Issue: Due to MicroScan autoSCAN-4 Instruments being manufactured with an incorrect...

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· 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· 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· 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· Boston Scientific Corporation

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

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 RADIOLOGY PROCEDURE 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 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 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