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. 2,442 recalls have been distributed to South Dakota in the last 12 months.

47,632 total recalls
2,442 in last 12 months

Showing 1702117040 of 47,632 recalls

FoodAugust 10, 2020· Whole Foods Market

Recalled Item: Whole Foods Market Chimay Biere PLU 29351700000 Individual sliced cheese...

The Issue: Undeclared lysozyme (from egg whites)

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodAugust 10, 2020· Whole Foods Market

Recalled Item: Whole Foods Market Chimay Grand Cru PLU 29388800000 and Whole Recalled by...

The Issue: Undeclared lysozyme (from egg whites)

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodAugust 10, 2020· Whole Foods Market

Recalled Item: Whole Foods Market Artequeso Manchego 6 month aged raw Raw Recalled by Whole...

The Issue: Undeclared lysozyme (from egg whites)

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodAugust 10, 2020· Whole Foods Market

Recalled Item: Whole Foods Market IL FORTETO Genovese Pesto PLU 20017100000 Individual...

The Issue: Undeclared lysozyme (from egg whites)

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodAugust 10, 2020· Whole Foods Market

Recalled Item: Whole Foods Market La Marquesa Herb Manchego Raw Milk - Recalled by Whole...

The Issue: Undeclared lysozyme (from egg whites)

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodAugust 10, 2020· Whole Foods Market

Recalled Item: Whole Foods Market AGRIFORM PIAVE VECCHIO PLU 29336200000 Individual sliced...

The Issue: Undeclared lysozyme (from egg whites)

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodAugust 10, 2020· Whole Foods Market

Recalled Item: Whole Foods Market El Trigal 12 Month Old Manchego PLU 29329500000 Recalled...

The Issue: Undeclared lysozyme (from egg whites)

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodAugust 10, 2020· Whole Foods Market

Recalled Item: Whole Foods Market Mitica Mahon PLU 29341800000 Individual sliced cheese...

The Issue: Undeclared lysozyme (from egg whites)

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
DrugAugust 7, 2020· Open Book Extracts

Recalled Item: Just Hand Sanitizer (Ethyl Alcohol 73%) Single Use-Packs 100-count NDC...

The Issue: Labeling Not Elsewhere Classified: Product labeled to contain methanol

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugAugust 7, 2020· Open Book Extracts

Recalled Item: Always Be Clean Hand Sanitizer (73% Alcohol) 0.04 FL OZ Recalled by Open...

The Issue: Labeling Not Elsewhere Classified: Product labeled to contain methanol

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugAugust 7, 2020· Santa Cruz Biotechnology, Inc

Recalled Item: UltraCruz Hand Sanitizing Gel Antimicrobial (70% Isopropyl Alcohol) Recalled...

The Issue: Subpotent drug

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 7, 2020· Tosoh Bioscience Inc

Recalled Item: Tosoh Bioscience AIA-PACK BHCG Calibration Verification Test Set-In Vitro...

The Issue: Decreased stability for five (5) lots of Calibrator Sets and Calibration...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2020· Maquet Cardiovascular Us Sales, Llc

Recalled Item: Maquet/Getinge Rotaflow System Console US (115 V / 60 Hz) Recalled by Maquet...

The Issue: Instruction For Use (IFU) incorrect serial number of 90437000. It should...

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

Class III — Low RiskOngoing
Medical DeviceAugust 7, 2020· Tosoh Bioscience Inc

Recalled Item: Tosoh Bioscience AIA- PACK HCG Calibrator Set-In Vitro Diagnostic for...

The Issue: Decreased stability for five (5) lots of Calibrator Sets and Calibration...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2020· Inpeco S.A.

Recalled Item: Accelerator a3600 system with Sysmex XN-9000/XN-9100 Interface Module (dual...

The Issue: Firmware of the Sysmex XN-9000/XN-9100 Interface Module (IM) and of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2020· Inpeco S.A.

Recalled Item: Aptio Automation systems with Sysmex XN-9000/XN-9100 Interface Module (dual...

The Issue: Firmware of the Sysmex XN-9000/XN-9100 Interface Module (IM) and of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2020· Boston Scientific Corporation

Recalled Item: WallFlexTM Biliary RX Fully Covered Stent System RMV (10mmx60mm Stent)...

The Issue: Mislabeled: WallFlex Biliary RX Uncovered Stent System 10x60mm devices...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2020· Inpeco S.A.

Recalled Item: FlexLab (FLX) with Sysmex XN-9000/XN-9100 Interface Module (dual robot)...

The Issue: Firmware of the Sysmex XN-9000/XN-9100 Interface Module (IM) and of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2020· TELEFLEX MEDICAL INC

Recalled Item: Pleur-evac Thoracic Catheters Catalog No: DTRC-20S The thoracic catheter is...

The Issue: Potential sterility issue

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2020· C-RAD POSITIONING AB

Recalled Item: PC Application Software c4D as part of the device Catalyst: Recalled by...

The Issue: PC Application Software c4D not changing Site upon synchronization during...

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

Class II — Potential Health HazardOngoing