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. 1,062 recalls have been distributed to South Dakota in the last 12 months.
Showing 5661–5680 of 27,558 recalls
Recalled Item: Veran : Endobronchial Models: INS-5500 View Optical Probe INS-5450 SPiN...
The Issue: Non-conformances in Veran devices (ig4 Image Guided System, SPiN Thoracic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Veran : Percutaneous Always on Track Models: INS-5040 Always-On vTrack...
The Issue: Non-conformances in Veran devices (ig4 Image Guided System, SPiN Thoracic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow ErgoPack Recalled by ARROW INTERNATIONAL Inc. Due to This recall has...
The Issue: This recall has been initiated due to reports that the product code and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Welch Allyn Connex Spot Monitor Recalled by Baxter Healthcare Corporation...
The Issue: Product is being recalled due to the improper placement of a copper tape on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: McGrath Mac 2 Recalled by Covidien Due to Laryngoscope blades may contain an...
The Issue: Laryngoscope blades may contain an ineffective application of anti-fog agent...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Veran : Endobronchial Always on Track Models: INS-0392 AOTT 21ga Needle...
The Issue: Non-conformances in Veran devices (ig4 Image Guided System, SPiN Thoracic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Guardian 2 System Product Name: Guardian System 2 Recalled by...
The Issue: A software update corrected an issue where "low" and "terminal" battery...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proboscis/Piston Assembly Recalled by Ortho-Clinical Diagnostics, Inc. Due...
The Issue: Ortho Clinical Diagnostics (QuidelOrtho) confirmed certain Proboscis/Piston...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 10ML SYRINGE LUER LOCK W/OUT NEEDLE Recalled by Fresenius Medical Care...
The Issue: There is a potential for blood backfill leakage and foreign material.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 10ML SYRINGE LUER LOCK W/NEEDLE Recalled by Fresenius Medical Care Holdings,...
The Issue: There is a potential for blood backfill leakage and foreign material.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3ML Syringe Luer Lock with needle 20GX1 Recalled by Fresenius Medical Care...
The Issue: There is a potential for blood backfill leakage and foreign material.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centered Glenosphere w/Screw Recalled by FX SHOULDER Due to Centered...
The Issue: Centered glenosphere box may contain an eccentric glenosphere.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oculus Myopia Master Recalled by Oculus Optikgeraete GMBH Due to Their is a...
The Issue: Their is a potential that optical devices with insufficient anti- coating...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Chemistry Iron_2 (IRON_2) Reagents Recalled by Siemens Healthcare...
The Issue: There is a potential for a positive bias on Quality Control (QC) and patient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oculus Pentacam AXL Wave Recalled by Oculus Optikgeraete GMBH Due to Their...
The Issue: Their is a potential that optical devices with insufficient anti- coating...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oculus Pentacam AXL Recalled by Oculus Optikgeraete GMBH Due to Their is a...
The Issue: Their is a potential that optical devices with insufficient anti- coating...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker ACM (Advanced Cement Mixing)System: ACM Kit w/ Femoral Breakaway...
The Issue: Potential for the Break-Away Femoral Nozzle the applicator tip connecting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Heartmate 3 LVAS Implant Kit Recalled by Thoratec Corp. Due to Inability to...
The Issue: Inability to start and/or complete the coring procedure due to inadequate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker ACM (Advanced Cement Mixing) System: ACM Kit w/ Femoral Recalled by...
The Issue: Potential for the Break-Away Femoral Nozzle the applicator tip connecting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker ACM (Advanced Cement Mixing)System: ACM Kit w/ Femoral Breakaway...
The Issue: Potential for the Break-Away Femoral Nozzle the applicator tip connecting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.