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. 1,783 recalls have been distributed to South Dakota in the last 12 months.
Showing 29821–29840 of 47,632 recalls
Recalled Item: LIFEPAK 15 Monitor Recalled by Physio-Control, Inc. Due to The firm has...
The Issue: The firm has become aware of a potential device issue where the LIFEPAK 15...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Carestream DRX-Revolution Mobile X-Ray System Recalled by Carestream Health...
The Issue: The firm received a complaint alleging that a DRX Revolution System could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Boston Scientific Recalled by Boston Scientific Corporation Due to There is...
The Issue: There is a potential for radio frequency (RF) interference to alter wireless...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trail's End Chicago Cubs Sweet and Savory Collection Trail's End Recalled by...
The Issue: Product has the potential to be contaminated with Salmonella
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Gift Sets with Chocolate Pretzel Dippers Recalled by Robert Rothschild Farm...
The Issue: The product is not labeled with an ingredient statement and therefore, does...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Gift Sets with Pretzel Twists Recalled by Robert Rothschild Farm LLC Due to...
The Issue: The product is not labeled with an ingredient statement and therefore, does...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Vertebral Motion Analyzer (VMA) Version 2.3.252. VMA software is a Recalled...
The Issue: Ortho Kinematics Inc. sent a Notice of Correction to Released Testing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: L-Varlock Cage/Trial Implant Holder Recalled by Kiscomedica S.A. Due to Firm...
The Issue: Firm received a complaint of the tip holder breaking during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vascular catheter introduction kit The PICC is indicated for short Recalled...
The Issue: There have been complaints for peel away sheaths flaring
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: N Latex HCY REAGENT Recalled by Siemens Healthcare Diagnostics, Inc. Due to...
The Issue: The firm confirmed a reduced once-opened and on-board stability for N Latex...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mammomat Inspiration full Recalled by Siemens Medical Solutions USA, Inc Due...
The Issue: Software error
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens ADVIA Centaur Systems Calibrator A Kits Recalled by Siemens...
The Issue: Siemens Healthcare Diagnostics has confirmed a negative bias for ADVIA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens ADVIA Centaur Systems Calibrator A Kits Recalled by Siemens...
The Issue: Siemens Healthcare Diagnostics has confirmed a negative bias for ADVIA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens ADVIA Centaur Systems Calibrator A Kits Recalled by Siemens...
The Issue: Siemens Healthcare Diagnostics has confirmed a negative bias for ADVIA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LIMA Modular Revision Hip Stem Model 428-01-050_110 Product Usage: The...
The Issue: Lima Proximal Bodies were inadvertently re-sterilized. The safety screw...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Empowr PS Knee Tibial Insert Recalled by Encore Medical, Lp Due to The...
The Issue: The Empowr PS Insert was reported as missing the impaction slot feature.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monaco RTP System. Used to make treatment plans for patients Recalled by...
The Issue: Incorrect dose after editing beam number an wedge angle.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Docetaxel Injection USP Recalled by Dr. Reddy's Laboratories, Inc. Due to...
The Issue: Defective Container: Product complaints received of defect in the seal of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Palmer's Candies Swirled Pretzels NET WT 5 OZ (141 g) packaged in foil bags...
The Issue: Product contains an ingredient that was recalled by a supplier because it...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Palmer's Candies Peppermint Bark A) NET WT 9 OZ (255 Recalled by Palmer and...
The Issue: Product contains an ingredient that was recalled by a supplier because it...
Recommended Action: Do not consume. Return to store for a refund or discard.