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. 2,360 recalls have been distributed to South Dakota in the last 12 months.
Showing 25341–25360 of 27,558 recalls
Recalled Item: Codman Certas Programmable Valve In Line Valve Only Product Code: Recalled...
The Issue: Codman Certas Programmable Valves used for hydrocephalus may not operate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CoaguChek XS System (HCP) The CoaguChek XS System is intended Recalled by...
The Issue: Roche has confirmed the potential for an undetected elevated INR test result...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Superstand stand-up wheelchair HPS-2 A standup wheelchair is a device...
The Issue: Power Superstand Standing Wheel chair, flex shaft (the flexible wand which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Codman Certas Programmable Valve In Line Valve with Unitized BactiSeal...
The Issue: Codman Certas Programmable Valves used for hydrocephalus may not operate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Codman Certas Programmable Valve In Line Valve with Siphonguard Recalled by...
The Issue: Codman Certas Programmable Valves used for hydrocephalus may not operate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Codman Certas Programmable Valve In Line Valve with SiphonGuard Device...
The Issue: Codman Certas Programmable Valves used for hydrocephalus may not operate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Codman Certas Programmable Valve In Line Valve with SiphonGuard Device...
The Issue: Codman Certas Programmable Valves used for hydrocephalus may not operate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CoaguChek XS Pro System The CoaguChek XS Pro System (CoaguChek Recalled by...
The Issue: Roche has confirmed the potential for an undetected elevated INR test result...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Codman Certas Programmable Valve In Line Valve only with SiphonGuard...
The Issue: Codman Certas Programmable Valves used for hydrocephalus may not operate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Codman Certas Programmable Valve In Line Valve with Catheter and Recalled by...
The Issue: Codman Certas Programmable Valves used for hydrocephalus may not operate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CoaguChek XS Plus System The CoaguChek XS Plus system for Recalled by Roche...
The Issue: Roche has confirmed the potential for an undetected elevated INR test result...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CoaguChek XS System (PST) The CoaguChek XS PT test strips Recalled by Roche...
The Issue: Roche has confirmed the potential for an undetected elevated INR test result...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AGFA Digital Radiography X-Ray System DX-D 100 Agfa's DX-D 100 Recalled by...
The Issue: Customers could potentially experience intermittent, unintended and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AIA Analyzer Pipette Tips used on Tosoh AIA-2000 Recalled by Tosoh Smd Inc...
The Issue: Visual inspection of the pipette tips indicated that some of the tips were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Superior Approach Resection Guide Assembly. Indicated for primary Recalled...
The Issue: Biomet has initiated this action following an investigation which identified...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Comfort brand Ear-Loop Face Mask Recalled by Maytex Corp Due to Recent Lab...
The Issue: Recent Lab testing conducted in March 2013 indicates that the product does...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Four Lead Arthroscopic Irrigation Set Recalled by Baxter Healthcare Corp....
The Issue: A firm's internal investigation led to the discovery of pinholes in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Four Lead TUR irrigation Set Recalled by Baxter Healthcare Corp. Due to A...
The Issue: A firm's internal investigation led to the discovery of pinholes in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: pocH-100i Recalled by Sysmex America Inc Due to The data printed on the...
The Issue: The data printed on the thermal printer may omit a digit or decimal point in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Two Lead Arthroscopic Irrigation Set Recalled by Baxter Healthcare Corp. Due...
The Issue: A firm's internal investigation led to the discovery of pinholes in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.