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 8101–8120 of 27,558 recalls
Recalled Item: Product Name: TEG5000 Analyzer (07-022 Recalled by Haemonetics Corporation...
The Issue: When the TEG 5000 Analyzer including TEG Analytical Software is used with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LEGION NARROW PS OXIN SZ 6N RT and JRNY II BCS FEMORAL OXIN LT SZ 5 Recalled...
The Issue: It was reported that a JOURNEY II BCS Femoral OXIN LT SZ5 was in a box...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medfusion Syringe Pump Models: 3500 Recalled by Smiths Medical ASD Inc. Due...
The Issue: Multiple issues with the potential for interruption of therapy or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medfusion Syringe Pump Model: Model 4000-0100-50 Recalled by Smiths Medical...
The Issue: Multiple issues with the potential for interruption of therapy or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Replacement back up batteries distributed on or after April 1 Recalled by GE...
The Issue: Insufficient battery backup power resulting in premature shutdown of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Back up batteries in Ventilators labeled as the following: a. Recalled by GE...
The Issue: Insufficient battery backup power resulting in premature shutdown of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: progenamatrix Human Keratin Matrix Recalled by ProgenaCare Due to Inner...
The Issue: Inner pouch seal may be inadequate resulting in lack of sterility.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Turbett Surgical Container Recalled by Turbett Surgical, Inc. Due to Devices...
The Issue: Devices were subject to unapproved rework processes.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartWare HVAD Pump Implant Kit Recalled by Medtronic Inc Due to The pump...
The Issue: The pump may have a welding defect that can lead the pump to malfunction....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BioPlex 2200 ToRC IgM Reagent Pack Recalled by Bio-Rad Laboratories, Inc....
The Issue: Performance concerns for the CMV IgM analyte. Analyte has demonstrated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: putty i-FACTOR Peptide Enhanced Bone Graft 1.0cc Syringe Recalled by...
The Issue: Patient chart label contains incorrect Part Number and volume amount.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica IM 1300 Analyzer - automated Recalled by Siemens Healthcare...
The Issue: Lots incompatible with Test Definition (TDef) Version 1.4, potentially lead...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica IM 1600 Analyzer - automated Recalled by Siemens Healthcare...
The Issue: Lots incompatible with Test Definition (TDef) Version 1.4, potentially lead...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Getinge CM320 WUWD Series Washer Disinfector-For use as a multi-chamber...
The Issue: Verification of installation not documented or may be incomplete, could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sensis Recalled by Siemens Medical Solutions USA, Inc Due to Siemens has...
The Issue: Siemens has become aware of three potential software issues with AXIOM...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AUTOLITH Touch 1.9F 375cm Biliary Electrohydraulic Lithotripter Probe...
The Issue: Product labeled incorrectly.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Getinge CM320-2 CHAMBER WU Series Washer Disinfector- For Use as Recalled by...
The Issue: Verification of installation not documented or may be incomplete, could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Crome Models loaded with CareLink SmartSync Device Manager application...
The Issue: Telemetry error that may occur with Medtronic Cobalt and Crome implantable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cobalt Models loaded with CareLink SmartSync Device Manager application...
The Issue: Telemetry error that may occur with Medtronic Cobalt and Crome implantable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis icono biplane -angiography systems developed for single and biplane...
The Issue: if the protective earth is interrupted and an additional fault leads to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.