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. 2,349 recalls have been distributed to South Dakota in the last 12 months.
Showing 26601–26620 of 47,632 recalls
Recalled Item: Halyard Closed Suction System for Adults Recalled by Halyard Health, Inc Due...
The Issue: Received recall notification from Smiths Medical that lots of 15ml Saline...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Halyard Turbo-Cleaning Closed Suction System for Adults Recalled by Halyard...
The Issue: Received recall notification from Smiths Medical that lots of 15ml Saline...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allen Medical Bow Frame Model A-70800. Surgical platform used to Recalled by...
The Issue: The base of the frame has the potential to crack when the patient is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Halyard Closed Suction System for Adults with BALLARD Technology WET...
The Issue: Received recall notification from Smiths Medical that lots of 15ml Saline...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: WECK(R) from TELEFLEX Auto Endo5(R) Recalled by Teleflex Medical Due to The...
The Issue: The product has a non-conformity that may cause clips to mislead, jam or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2008T Recalled by Fresenius Medical Care Renal Therapies Group, LLC Due to...
The Issue: While reviewing documentation for the next software release of the 2008T, an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MONTERIS MEDICAL NEUROBLATE SYSTEM Recalled by Monteris Medical Corp Due to...
The Issue: The firm received complaints that involved an unanticipated interaction...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Network Firewall (Cisco ASA 5506) Recalled by Philips Electronics...
The Issue: Firewall installed with Philips IntelliVue Information Center iX or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Betadine Solution Swabstick Povidone-Iodine Solution USP Recalled by Purdue...
The Issue: Subpotent Drug: The laminate used to make the pouches was reversed such that...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Famotidine tablets Recalled by Dr. Reddy's Laboratories, Inc. Due to Failed...
The Issue: Failed impurities/degradation specifications: Famotodine has an out of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: iBalance(R) UKA Recalled by Arthrex, Inc. Due to Arthrex part number...
The Issue: Arthrex part number AR-501-UFLC, size 3, batch 10123297, has the incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Difco" Agar Noble Recalled by Becton Dickinson & Co. Due to Mislabeling
The Issue: HighPuragar was mislabeled and inadvertently sold as Noble Agar.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Go.Now computed tomography (CT) x-ray system table Recalled by...
The Issue: The table may become unstable if the nuts on the bolts were not adequately...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hemosphere System with the following three components: HEM1 Advanced Monitor...
The Issue: Pre-procedural issues related to software defects
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Go.Up computed tomography (CT) x-ray system table Recalled by...
The Issue: The table may become unstable if the nuts on the bolts were not adequately...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bisoprolol Fumarate tablets Recalled by Unichem Pharmaceuticals Usa Inc Due...
The Issue: Failed Impurities/Degradation Specifications: Out of Specification for an...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: O-arm¿ O2 interventional fluoroscopic x-ray system Recalled by Medtronic...
The Issue: During servicing of certain internal components of the O-Arm O2 Surgical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vanguard Complete Knee System Recalled by Zimmer Biomet, Inc. Due to Knee...
The Issue: Knee implant components (tibial bearings) are labeled with the incorrect size.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vanguard Complete Knee System Recalled by Zimmer Biomet, Inc. Due to Knee...
The Issue: Knee implant components (tibial bearings) are labeled with the incorrect size.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Birds Eye Baby Sweet Peas Recalled by Pinnacle Food Group, Llc Due to...
The Issue: Product has the potential to be contaminated with Listeria monocytogenes.
Recommended Action: Do not consume. Return to store for a refund or discard.