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. 2,429 recalls have been distributed to South Dakota in the last 12 months.
Showing 19361–19380 of 27,558 recalls
Recalled Item: Conserve Shells: Recalled by MicroPort Orthopedics Inc. Due to Revision rate...
The Issue: Revision rate trends from within the MicroPort Orthopedics Inc. database...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PoleStar system (N20 / N30) Warning Lamps Control Box Recalled by Medtronic...
The Issue: Medtronic Navigation is recalling certain components of the PoleStar system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Achillon Minimally Invasive Device for Achilles Tendon Rupture Treatment The...
The Issue: Data from internal studies suggests there may be a potential that the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Recalled by Medtronic Inc., Cardiac Rhythm and Heart Failure Due...
The Issue: This Pacing Lead System does not comply with Section 8.5.2.3 of IEC 60601-1,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5.0mm Round Fluted Bur Recalled by Stryker Instruments Div. of Stryker...
The Issue: Stryker Instruments initiated a voluntary recall of specific lots of Round...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AB Sciex API 3200MD" LC/MS/MS System. In-Vitro Diagnostic Instrument Part...
The Issue: MultiQuant MD software where under certain conditions a user can be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 6.0mm Round Fluted Bur Recalled by Stryker Instruments Div. of Stryker...
The Issue: Stryker Instruments initiated a voluntary recall of specific lots of Round...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AB SCIEX QTRAP¿ 4500MD LC/MS/MS System Mass Spectrometer for In-Vitro...
The Issue: MultiQuant MD software where under certain conditions a user can be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AB SCIEX 3200MD QTRAP¿ LC/MS/MS System Mass Spectrometer for In-Vitro...
The Issue: MultiQuant MD software where under certain conditions a user can be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AB SCIEX Triple Quad 4500MD LC/MS/MS System. Mass Spectrometer for Recalled...
The Issue: MultiQuant MD software where under certain conditions a user can be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A7 Anesthesia Delivery System Recalled by Mindray DS USA, Inc. dba Mindray...
The Issue: Potential for a leak to occur on the back-up O2 and air e-size cylinder...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith and Nephew TWINFIX QUICK-T Knot Pusher Suture Cutter Recalled by Smith...
The Issue: The device could be subject to breaches of its sterile packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: T100-022WF Recalled by WalkMed Infusion, LLC Due to WalkMed Infusion, LLC...
The Issue: WalkMed Infusion, LLC Announces a Voluntary Field Action of Multiple Triton...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: T105-000WC IV Set w/2 Y-Sites Recalled by WalkMed Infusion, LLC Due to...
The Issue: WalkMed Infusion, LLC Announces a Voluntary Field Action of Multiple Triton...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: T095-120 IV Set with 1.2 Micron Filter. Packaged in a Tyvek pouch Recalled...
The Issue: WalkMed Infusion, LLC Announces a Voluntary Field Action of Multiple Triton...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: T100-000WF Recalled by WalkMed Infusion, LLC Due to WalkMed Infusion, LLC...
The Issue: WalkMed Infusion, LLC Announces a Voluntary Field Action of Multiple Triton...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The pump (with cushioning foam inserts) is packaged in a Recalled by WalkMed...
The Issue: WalkMed Infusion, LLC Announces a Voluntary Field Action of the Triton...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: T100-022F with 0.22 micron filter and FP Clip. Packaged in a Tyvek pouch...
The Issue: WalkMed Infusion, LLC Announces a Voluntary Field Action of Multiple Triton...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The pump (with cushioning foam inserts) is packaged in a Recalled by WalkMed...
The Issue: WalkMed Infusion, LLC Announces a Voluntary Field Action of the Triton...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: T100-120F with 1.2 micron filter and FP Clip. Packaged in a Tyvek pouch...
The Issue: WalkMed Infusion, LLC Announces a Voluntary Field Action of Multiple Triton...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.