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. 2,467 recalls have been distributed to South Dakota in the last 12 months.
Showing 14481–14500 of 27,558 recalls
Recalled Item: VITROS NT-proBNP Reagent Recalled by ORTHO-CLINICAL DIAGNOSTICS Due to The...
The Issue: The firm is extending their previous July 2018 recall to include additional...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Anti-HBe Reagent Pack Recalled by ORTHO-CLINICAL DIAGNOSTICS Due to...
The Issue: The firm is extending their previous July 2018 recall to include additional...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Quantikine¿ IVD¿ ELISA Recalled by R & D Systems, Inc. Due to The Human sTfR...
The Issue: The Human sTfR Quantikine IVD ELISA Kit, catalog # DTFR1, lot P180151 was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The SQ-RX Pulse Generator a component of the Subcutaneous Implantable...
The Issue: Experienced accelerated battery depletion and a shortened replacement...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SORIN Heater-Cooler System 3T 120V~/60Hz Description of product: Recalled by...
The Issue: The firm has become aware that due to a chemical reaction, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Protexis Neoprene Surgical Glove Recalled by Cardinal Health 200, LLC Due to...
The Issue: Labeling issue in that the breakthrough (i.e., permeation) times for two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Protexis Neoprene Surgical Glove Recalled by Cardinal Health 200, LLC Due to...
The Issue: Labeling issue in that the breakthrough (i.e., permeation) times for two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NexGen¿ Complete Knee Solution Femoral Augment Block Distal only Recalled by...
The Issue: Screw is missing from the package
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FoundationOne CDx Test Results Recalled by Foundation Medicine, Inc. Due to...
The Issue: An incorrect test result for a single analyte may have been reported for up...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Protexis Neoprene Surgical Glove Recalled by Cardinal Health 200, LLC Due to...
The Issue: Labeling issue in that the breakthrough (i.e., permeation) times for two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Salem Sump Dual Lumen Stomach Tube 10 Fr/Ch (3.3 mm) x 36" (91 cm) Recalled...
The Issue: This voluntary recall is being conducted due to incorrect packaging. In one...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Protexis Neoprene Surgical Glove Recalled by Cardinal Health 200, LLC Due to...
The Issue: Labeling issue in that the breakthrough (i.e., permeation) times for two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Protexis Neoprene Surgical Glove Recalled by Cardinal Health 200, LLC Due to...
The Issue: Labeling issue in that the breakthrough (i.e., permeation) times for two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Protexis Neoprene Surgical Glove Recalled by Cardinal Health 200, LLC Due to...
The Issue: Labeling issue in that the breakthrough (i.e., permeation) times for two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Protexis Neoprene Surgical Glove Recalled by Cardinal Health 200, LLC Due to...
The Issue: Labeling issue in that the breakthrough (i.e., permeation) times for two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Protexis Neoprene Surgical Glove Recalled by Cardinal Health 200, LLC Due to...
The Issue: Labeling issue in that the breakthrough (i.e., permeation) times for two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QUADROX-i Neonatal with integrated arterial filter and VHK 11000 (VKMO...
The Issue: There is a potential for blood leakage at the blood inlet connector when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QUADROX-i Neonatal without integrated arterial filter and VHK 11000 (VKMO...
The Issue: There is a potential for blood leakage at the blood inlet connector when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biomet 20mm Compress Device Short Anchor Plug With Drill Set Recalled by...
The Issue: Potential metal burrs in the holes of the device preventing the appropriate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Natural Nail¿ System - Tear Drop Guide Wire Recalled by Zimmer...
The Issue: Various Trauma Guide Wires- creases in the sealing area on the end opposite...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.