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. 2,360 recalls have been distributed to South Dakota in the last 12 months.
Showing 25941–25960 of 27,558 recalls
Recalled Item: D3000 Advantage Drive System Recalled by Linvatec Corp. dba ConMed Linvatec...
The Issue: The Membrane Switch Panel ( to as "front panel" of the component part number...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stelkast Cross-over Acetabular Shell and Liner Hip System Recalled by...
The Issue: Firm was made aware of incidents relating to the difficulty of properly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Plastic bottle containing 10.5 mL of IgM Conjugate Product Usage: Recalled...
The Issue: Affected products have a labeled expiration date of one year too long.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: USHER¿ Support Catheter- Angled Tip WL130cm Recalled by Bard Peripheral...
The Issue: Bard Peripheral Vascular (BPV) is initiating this recall because a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BARD Biopsy Systems (A Business Unit of Bard Peripheral Vascular Recalled by...
The Issue: Bard Peripheral Vascular (BPV) is initiating this recall because a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Plastic bottle containing 10.5 mL of IgG Conjugate Product Usage: Recalled...
The Issue: Affected products have a labeled expiration date of one year too long.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BARD Biopsy Systems (A Business Unit of Bard Peripheral Vascular Recalled by...
The Issue: Bard Peripheral Vascular (BPV) is initiating this recall because a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MICROSHEATH¿ - 0.066 (1.7mm) proximal Recalled by Bard Peripheral Vascular...
The Issue: Bard Peripheral Vascular (BPV) is initiating this recall because a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Plastic bottle containing 3.5 mL of IgG FITC Conjugate Product Recalled by...
The Issue: Affected products have a labeled expiration date of one year too long.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardinal Health hCG Cassette Rapid Test Recalled by Alere San Diego, Inc....
The Issue: Alere San Diego Inc. is recalling the Cardinal Health hCG Cassette Rapid...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Advantx Recalled by GE Healthcare, LLC Due to A locking nut...
The Issue: A locking nut might loosen out of the overhead Video Monitor Suspension yoke...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lifeguard Infusion Set with Smartsite Recalled by Churchill Medical Systems,...
The Issue: The label on the device states that the item number is CLGY-2210 when the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Chenica Gunnell Rehab Series of Wheelchairs (GRSW) Recalled by CHENICA INC....
The Issue: The wheelchairs may not meet the specifications of WC-19 (crash testing),...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aesculap Bipolar Generator Foot Pedal Recalled by Aesculap, Inc. Due to The...
The Issue: The bipolar energy did not stop after release of the foot pedal.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Elekta Recalled by Elekta, Inc. Due to If the Apex collimator is incorrectly...
The Issue: If the Apex collimator is incorrectly installed on the radiation head, a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: St. Jude Medical Recalled by St Jude Medical Inc Due to The distal end of...
The Issue: The distal end of the core wire of the TorqVue FX Delivery System could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SybronEndo Replacement AC Power Cord Recalled by Ormco/Sybronendo Due to A...
The Issue: A recall has been issued by SybronEndo because a Canadian Standards...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SybronEndo Elements Obturation Unit Recalled by Ormco/Sybronendo Due to A...
The Issue: A recall has been issued by SybronEndo because a Canadian Standards...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KODAK INSIGHT DENTAL FILM in SureSoft Packets Recalled by Carestream Health,...
The Issue: Missing symbols and manufacturing information on the clear carton label. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips BuckyDiagnost Radiographic. Catalog Numbers: 704031 Recalled by...
The Issue: An inspection of IATD (Installation Acceptance Test Document)IA SID (Source...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.