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. 2,465 recalls have been distributed to South Dakota in the last 12 months.
Showing 14801–14820 of 27,558 recalls
Recalled Item: Hoffman LRF Hexapod Strut Recalled by Stryker GmbH Due to The press fit...
The Issue: The press fit connection of the Angular Sleeve and pin of the U-Joint and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Immunodiagnostic Products Vitamin B12 Reagent Pack 1/2 Recalled by...
The Issue: The reagent pack exhibits the potential for an increased frequency of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hoffman LRF Hexapod Strut Recalled by Stryker GmbH Due to The press fit...
The Issue: The press fit connection of the Angular Sleeve and pin of the U-Joint and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abbott ARCHITECT cSystems ICT Module Recalled by Abbott Laboratories, Inc...
The Issue: There is a potential to generate falsely elevated serum or plasma chloride...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Li-ion Battery Housing for AR-400 DrillSaw Sports 400 System Product...
The Issue: The Li-ion Battery Housing for the AR-400 DrillSaw Sports 400 System may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gibco MEM Non-Essential Amino Acids Solution (100X) (SKU 11140050) Recalled...
The Issue: Leaky bottles due to a defect in the bottle cap compromising the sterility...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gibco DPBS Recalled by Life Technologies, Corp. Due to Leaky bottles due to...
The Issue: Leaky bottles due to a defect in the bottle cap compromising the sterility...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gibco GlutaMAX Supplement Recalled by Life Technologies, Corp. Due to Leaky...
The Issue: Leaky bottles due to a defect in the bottle cap compromising the sterility...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integrated Gate Controller PCB (component of AlignRT Plus) Truebeam variant...
The Issue: RTInterface error in the event of an I/O error between the IGC PCB and the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gibco Sodium Pyruvate (100 mM) SKU 11360070 Recalled by Life Technologies,...
The Issue: Leaky bottles due to a defect in the bottle cap compromising the sterility...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Beckman Coulter Lipase Recalled by Beckman Coulter Inc. Due to NAPQI, a...
The Issue: NAPQI, a metabolite of Acetaminophen, causes negative interference with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Beckman Coulter Uric Acid Recalled by Beckman Coulter Inc. Due to NAPQI, a...
The Issue: NAPQI, a metabolite of Acetominophen, causes negative interference with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD NEXIVA Closed IV Catheter System Dual Port 18GA 1.25 IN (BD Nexiva...
The Issue: One lot of the specified needles is not performing as intended due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AIA-360 Analyzer Recalled by Tosoh Bioscience Inc Due to The firm has...
The Issue: The firm has implemented new product labeling changes for the Tosoh AIA-360...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Jelco(R) ViaValve(TM) safety intravenous (I.V.) catheters Recalled by Smiths...
The Issue: Several lots of Jelco¿ ViaValve" safety intravenous (I.V.) catheters...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biomet Microfixation RapidFlap System 20MM RapidFlap SpinDown Clamp :...
The Issue: Spin Down RapidFlap nut that interfaces with the outer plate was assembled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biomet Microfixation RapidFlap System 16MM RapidFlap SpinDown Clamp Recalled...
The Issue: Spin Down RapidFlap nut that interfaces with the outer plate was assembled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biomet Microfixation RapidFlap System 20MM RapidFlap SpinDown Clamp Recalled...
The Issue: Spin Down RapidFlap nut that interfaces with the outer plate was assembled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biomet Microfixation RapidFlap System Recalled by Zimmer Biomet, Inc. Due to...
The Issue: Spin Down RapidFlap nut that interfaces with the outer plate was assembled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biomet Microfixation RapidFlap System 12mm SpinDown Clamp Recalled by Zimmer...
The Issue: Spin Down RapidFlap nut that interfaces with the outer plate was assembled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.