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. 2,259 recalls have been distributed to South Dakota in the last 12 months.
Showing 47221–47240 of 47,632 recalls
Recalled Item: BLOM-SINGER indwelling TEP Occluder Recalled by Helix Medical LLC Due to...
The Issue: Helix Medical LLC is recalling the BLOM-SINGER indwelling TEP Occluder due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pinnacle Hip Solutions ALTRX Polyethylene Acetabular Liner Recalled by DePuy...
The Issue: DePuy Orthopaedics, Inc. (DePuy) is issuing a voluntary recall of one lot of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: i-STAT cTnI cartridges Product Usage: The i-STAT cTnl test is Recalled by...
The Issue: Abbott Point of Care has determined that i-Stat CTNL cartridges have the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: S4 Cervical (S4C) Revision Instruments (FW099R and FW101R). The S4C Recalled...
The Issue: Aesculap Implant Systems, LLC has initiated a voluntary removal of the S4...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Quasar Nuclear Medicine System Recalled by GE Healthcare, LLC...
The Issue: Accelerated fatigue of the lateral axis motion subsystem of the Infinia...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Vacutainer PST Gel and Lithium Heparin (LH) Recalled by Becton Dickinson...
The Issue: BD is conducting a recall of the BD Vacutainer Plus Plastic Plasma Separator...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: I-STAT PT/INR cartridge Abbott Point of Care Inc. Abbott Park Recalled by...
The Issue: The i-STAT PT/INR cartridges have the potential to exhibit incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Thyro-Tab.075 mg. Recalled by Lloyd Inc Due to Subpotent (Single Ingredient...
The Issue: Subpotent (Single Ingredient Drug): Low assay at the 6-month test interval.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levothroid (levothyroxine sodium tablets Recalled by Lloyd Inc Due to...
The Issue: Subpotent (Single Ingredient Drug): Low assay at the 6-month test interval.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lithium Thionyl non-rechargeable disposable battery pack P/N 350-0294-01...
The Issue: Braemar has recently became aware of a battery related incident that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens syngo.plaza. Radiological image processing system Recalled by...
The Issue: Siemens became aware of a potential malfunction when using syngo.plaza with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Man King Capsules Recalled by www.vitaminbestbuy.com Due to Marketed Without...
The Issue: Marketed Without an Approved ANDA/NDA: presence of sildenafil.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Japan Weight Loss Blue Capsules Recalled by www.vitaminbestbuy.com Due to...
The Issue: Marketed Without an Approved ANDA/NDA: presence of sibutramine
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Hard Ten Days Capsule Recalled by www.vitaminbestbuy.com Due to Marketed...
The Issue: Marketed Without an Approved ANDA/NDA: presence of sildenafil
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Thyroglobulin Antibody (TgAB) Calibrator - Product Usage: intended for IN...
The Issue: Some combinations of Calibrator lots and AlA PACKS resulted in Calibrator #6...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TX1 Tissue Removal System Console. Model: TX1 TX1 Tissue Removal Recalled by...
The Issue: Two reasons for recall. 1. Incorrect pressure relief valve installed inside...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The brand name of the device is AlgiNot Recalled by Kerr Corporation Due to...
The Issue: The firm recalled the product because it may cure harder than expected...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Toshiba Ultra-Short Magnetic Resonance Imaging System Recalled by Toshiba...
The Issue: The firm recalled due to a potentail problem with the position of the hold...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Columbus Tibia Plateau (component of the Columbus REVISION Knee System)...
The Issue: During an internal quality inspection, the tibia plateau was found to be out...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FLOW-I Anesthesia System The system is intended for use in Recalled by...
The Issue: A technical alarm may be generated on the FLOW-i system when using the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.