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. 2,510 recalls have been distributed to South Dakota in the last 12 months.
Showing 10601–10620 of 27,558 recalls
Recalled Item: Medtronic Intellis Spinal Cord Stimulator Recalled by Medtronic...
The Issue: A710 Intellis Clinician Application has a software issue that can result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infinity ACL Tibial Tip Guide- indicated for use in open Recalled by ConMed...
The Issue: Tips of the Infinity ACL Tibial Elbow and Tip Guides are potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infinity ACL Tibial Elbow Guide-indicated for use in open and Recalled by...
The Issue: Tips of the Infinity ACL Tibial Elbow and Tip Guides are potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stimulan Kit 10cc Recalled by Biocomposites, Ltd. Due to Mislabeling
The Issue: The product is mislabeled.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Life2000 Ventilation System Recalled by Hill-Rom Manufacturing, Inc. Due to...
The Issue: Under certain conditions, there is a risk for fire.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Canon PET-CT SCANNER Recalled by Canon Medical System, USA, INC. Due to A...
The Issue: A software problem has been identified which could result in the diagnostic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by Westmed, Inc. Due to There is a potential that the fitment...
The Issue: There is a potential that the fitment between the oxygen delivery tube and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (Adult Elongated O2/CO2 Mask - Product Usage: intended Recalled by Westmed,...
The Issue: There is a potential that the fitment between the oxygen delivery tube and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Adult Elongated CO2/O2 Mask Recalled by Westmed, Inc. Due to There is a...
The Issue: There is a potential that the fitment between the oxygen delivery tube and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by Westmed, Inc. Due to There is a potential that the fitment...
The Issue: There is a potential that the fitment between the oxygen delivery tube and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by Westmed, Inc. Due to There is a potential that the fitment...
The Issue: There is a potential that the fitment between the oxygen delivery tube and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Westmed DISPOSABLE RESPIRATORY PRODUCTS NON-REBREATHER MASK Recalled by...
The Issue: There is a potential that the fitment between the oxygen delivery tube and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (1) Capiox FX25 (West) Advance Oxygenator- with left port Recalled by Terumo...
The Issue: Capiox FX25 Advance oxygenator may be the incorrect configuration (East vs....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation 4 Recalled by RAYSEARCH LABORATORIES AB Due to Two issues were...
The Issue: Two issues were found with the treatment plan report: 1) There may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Instruction Manual for Mayfield A2000 Skull Cap - Product Usage: Recalled by...
The Issue: Revised Instruction Manual to the most accurate illustration for Mayfield...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ELI 380 Electrocardiograph - Product Usage: intended to be a...
The Issue: The radio within the device can become disassociated with the wireless...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MiniCap Extended Life PD Transfer Set Recalled by Baxter Healthcare...
The Issue: Potential for no-flow and leaks under the twist clamp.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CryoValve SG Pulmonary Human Heart Valve. The valve is cryopreserved...
The Issue: On November 10, 2020, it was discovered that there are post- processing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMT Male ENFit-to-Stepped Male (Christmas Tree) Adapter Recalled by Applied...
The Issue: The products subject to this recall may contain obvious, incorrect pouch...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CryoPatch SG Pulmonary Human Cardiac Patch. The patch is cryopreserved...
The Issue: On November 10, 2020, it was discovered that there are post- processing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.