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. 2,516 recalls have been distributed to South Dakota in the last 12 months.
Showing 7541–7560 of 27,558 recalls
Recalled Item: Hammertoe Continuous Compression Implant (CCI) Kit Part Number: 46.239.001...
The Issue: Drill Pin (drill bit) is not compatible with the Drill Template included in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Iso-Gard Filter S Recalled by TELEFLEX LLC Due to Incidents of device...
The Issue: Incidents of device splitting or detaching during use
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Iso-Gard Filter S Recalled by TELEFLEX LLC Due to Incidents of device...
The Issue: Incidents of device splitting or detaching during use
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Iso-Gard Filter S Recalled by TELEFLEX LLC Due to Incidents of device...
The Issue: Incidents of device splitting or detaching during use
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Filter + Catheter Mount Recalled by TELEFLEX LLC Due to Incidents of device...
The Issue: Incidents of device splitting or detaching during use
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Iso-Gard Filter S Recalled by TELEFLEX LLC Due to Incidents of device...
The Issue: Incidents of device splitting or detaching during use
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Iso-Gard Filter S with Expandi-Flex/Elbow: a) Recalled by TELEFLEX LLC Due...
The Issue: Incidents of device splitting or detaching during use
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OSSUR Power Knee OSSUR Power Knee Recalled by Ossur Americas Due to Battery...
The Issue: Battery may dislodge from the Power Knee
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Leica Surgical Operating Microscopes Recalled by Leica Microsystems, Inc....
The Issue: During internal testing, Leica Microsystems has become aware of a component...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Leica Surgical Operating Microscopes Recalled by Leica Microsystems, Inc....
The Issue: During internal testing, Leica Microsystems has become aware of a component...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Leica Surgical Operating Microscopes Recalled by Leica Microsystems, Inc....
The Issue: During internal testing, Leica Microsystems has become aware of a component...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Leica Surgical Operating Microscopes Recalled by Leica Microsystems, Inc....
The Issue: During internal testing, Leica Microsystems has become aware of a component...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: G7 Acetabular System Recalled by Zimmer, Inc. Due to The outer sterile...
The Issue: The outer sterile package cavity has a corner wall thickness that is below...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista High Density Lipoprotein Cholesterol (HDLC) Flex reagent...
The Issue: Dimension Vista¿ High Density Lipoprotein Cholesterol (HDLC) Potential for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: sentec 24 / MARe-SF Multi-Site Attachment Ring Easy Recalled by SenTec AG...
The Issue: Weak skin adhesion.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Magnesium (MG) Flex reagent cartridge Siemens Material Number...
The Issue: Dimension Magnesium (MG) Flex reagent cartridge lots may exhibit imprecision...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fungitell STAT- IVD Assay for (1 ¿ 3)-~-D-Glucan in Serum Recalled by...
The Issue: Incorrect information on the Fungitell STAT clamshells containing the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ConvaTec Active Life Recalled by ConvaTec, Inc Due to impaired functionality...
The Issue: impaired functionality of the release liner
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ConvaTec Esteem+ Durahesive Plus Recalled by ConvaTec, Inc Due to impaired...
The Issue: impaired functionality of the release liner
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ConvaTec Esteem+ Durahesive Plus Recalled by ConvaTec, Inc Due to impaired...
The Issue: impaired functionality of the release liner
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.