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. 2,554 recalls have been distributed to South Dakota in the last 12 months.
Showing 2641–2660 of 47,632 recalls
Recalled Item: Brand Name: Ballard Product Name: Closed Suction Catheters Model/Catalog...
The Issue: Lack of sterility assurance for closed suction catheter systems
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Ballard Product Name: Closed Suction Catheters Model/Catalog...
The Issue: Lack of sterility assurance for closed suction catheter systems
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Ballard Product Name: Closed Suction Catheters Model/Catalog...
The Issue: Lack of sterility assurance for closed suction catheter systems
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Ballard Product Name: Closed Suction Catheters Model/Catalog...
The Issue: Lack of sterility assurance for closed suction catheter systems
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Ballard Product Name: Closed Suction Catheters Model/Catalog...
The Issue: Lack of sterility assurance for closed suction catheter systems
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: META-TAN LAG/COMPRESSION SCREW KIT 90MM/85MM Recalled by Smith & Nephew,...
The Issue: Integrated Lag/Compression Screw Kit has a compression screw with hexagon...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: CELL-DYN Ruby Product Name: CELL-DYN Ruby Model/Catalog Number:...
The Issue: When expired reagents are scanned or manually entered, the system will...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: CELL-DYN Ruby Product Name: CELL-DYN Ruby Model/Catalog Number:...
The Issue: When expired reagents are scanned or manually entered, the system will...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: CELL-DYN Ruby Product Name: CELL-DYN Ruby Model/Catalog Number:...
The Issue: When expired reagents are scanned or manually entered, the system will...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: CELL-DYN Ruby Product Name: CELL-DYN Ruby Model/Catalog Number:...
The Issue: When expired reagents are scanned or manually entered, the system will...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: CELL-DYN Ruby Product Name: CELL-DYN Ruby Model/Catalog Number:...
The Issue: When expired reagents are scanned or manually entered, the system will...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atorvastatin Calcium Tablets USP 40 mg Recalled by BIOCON PHARMA INC Due to...
The Issue: Failed dissolution specifications: lower than specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: DxC 500 AU Clinical Chemistry Analyzer Recalled by Beckman Coulter Inc. Due...
The Issue: The reason for the recall is incorrect sample barcode identification and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Amplatzer TorqVue LP Delivery System (TVLP) Recalled by Abbott Due to Device...
The Issue: Device may have a small breach in the proximal end of the shaft under the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Amplatzer TorqVue LP Catheter (TVLPC) Recalled by Abbott Due to Device may...
The Issue: Device may have a small breach in the proximal end of the shaft under the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Esaote Endocavity ultrasonic probe Recalled by ESAOTE S.P.A. Due to A...
The Issue: A potential weakness has been identified in the probe body, so that, in a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DORO¿ Easy-Connect Navigation Adaptor Recalled by Pro-Med Instruments Gmbh...
The Issue: Potential of compromised compatibility resulting in influence on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merit Medical Recalled by Merit Medical Systems, Inc. Due to Update to IFU...
The Issue: Update to IFU to provide additional information related to risk with device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merit Medical Recalled by Merit Medical Systems, Inc. Due to Update to IFU...
The Issue: Update to IFU to provide additional information related to risk with device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SeaBear Smokedhouse Salmon Chowder is packaged in flexible retort pouch...
The Issue: Recall was initiated due to potential failure of the seal and potential to...
Recommended Action: Do not consume. Return to store for a refund or discard.