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 8381–8400 of 47,632 recalls
Recalled Item: .14.800 Recalled by Limacorporate S.p.A Due to Due to manufacturing issue,...
The Issue: Due to manufacturing issue, their is a potential for peripheral holes to be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: .14.500 Recalled by Limacorporate S.p.A Due to Due to manufacturing issue,...
The Issue: Due to manufacturing issue, their is a potential for peripheral holes to be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Endoscope Reprocessor OER-Mini-For use in cleaning and high-level...
The Issue: Revised OER-Pro, OER-Elite, OER-Mini endoscope reprocessor labeling- the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tracheal Intubation Fiberscope OLYMPUS LF-P- To be used with an Recalled by...
The Issue: Revised OER-Pro, OER-Elite, OER-Mini endoscope reprocessor labeling- the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Endoscope Reprocessor OER-Elite-For use in cleaning and high-level...
The Issue: Revised OER-Pro, OER-Elite, OER-Mini endoscope reprocessor labeling- the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VISERA Tracheal Intubation Videoscope OLYMPUS LF Type V- For airway Recalled...
The Issue: Revised OER-Pro, OER-Elite, OER-Mini endoscope reprocessor labeling- the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Endoscope Reprocessor OER-Pro-For use in cleaning and high-level...
The Issue: Revised OER-Pro, OER-Elite, OER-Mini endoscope reprocessor labeling- the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abiomed 14Fr Low Profile Introducer Set Recalled by Abiomed, Inc. Due to...
The Issue: There was one complaint that the sidearm of the device detached during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Travoprost Ophthalmic Solution Recalled by Golden State Medical Supply Inc....
The Issue: Lack of Assurance of Sterility: Tamper Evidence Seal is missing on secondary...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: enterade Advanced Oncology Formula Recalled by ENTRINSIC HEALTH SOLUTION INC...
The Issue: Potential for the product to develop mold and spoil.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Flexiva Pulse 242 TracTip Single-Use Laser Fibers -intended to be Recalled...
The Issue: Manufactured with the incorrect component may result in lower power output...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flexiva Pulse 242 TracTip Single-Use Laser Fibers - intended to Recalled by...
The Issue: Manufactured with the incorrect component may result in lower power output...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flexiva Pulse ID-intended to be used as a device that Recalled by Boston...
The Issue: Manufactured with the incorrect component may result in lower power output...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flexiva Pulse 242 Single-Use Laser Fibers-intended to be used as Recalled by...
The Issue: Manufactured with the incorrect component may result in lower power output...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flexiva Pulse ID-intended to be used as a device that Recalled by Boston...
The Issue: Manufactured with the incorrect component may result in lower power output...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flexiva Pulse 242 ID Trac Single Use Fiber-intended to be Recalled by Boston...
The Issue: Manufactured with the incorrect component may result in lower power output...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flexiva Pulse ID 242 TracTip single Use Fiber-intended to be Recalled by...
The Issue: Manufactured with the incorrect component may result in lower power output...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Slick Set Uncuffed Endotracheal Tube and Stylet Set Recalled by TELEFLEX LLC...
The Issue: Reports of disconnection of the 15mm connector from the endotracheal tube...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy Recalled by...
The Issue: Reports of disconnection of the 15mm connector from the endotracheal tube...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endotracheal Tube oral/nasal Murphy Eye Recalled by TELEFLEX LLC Due to...
The Issue: Reports of disconnection of the 15mm connector from the endotracheal tube...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.