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. 2,365 recalls have been distributed to South Dakota in the last 12 months.
Showing 22561–22580 of 47,632 recalls
Recalled Item: Nutty Choco Pop Recalled by Funky Chunky LLC Due to Nutty Choco Pop has in...
The Issue: Nutty Choco Pop has in incorrect label and does not declare that it contains...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: The WinStation Retinal Imager Recalled by Merge Healthcare, Inc. Due to...
The Issue: Certain configurations of Merge Eye Station hardware may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Centricity Universal Viewer Breast Imaging Centricity...
The Issue: When switching back & forth between multiple UV instances in the Windows...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CoaguChek XS PT Test Recalled by TERRIFIC CARE LLC Due to Potential for...
The Issue: Potential for abnormally high INR test results with the CoaguChek XS PT Test...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olmesartan Medoxomil and Hydrochlorothiazide Tablets Recalled by Teva...
The Issue: Failed dissolution specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fungitell Kit Recalled by Associates of Cape Cod, Inc. Due to The kits may...
The Issue: The kits may contain the incorrect number of components or the kits may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Durex Pleasure Pack (60 ct) Recalled by Reckitt Benckiser LLC Due to Five...
The Issue: Five batches of the product have failed the specification of 1.0kPa for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Durex Real Feel Recalled by Reckitt Benckiser LLC Due to Five batches of the...
The Issue: Five batches of the product have failed the specification of 1.0kPa for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Entuit Secure Gastrointestinal Suture Anchor Set Recalled by Cook Inc. Due...
The Issue: There is a potential for difficulty in sliding down the retention mechanism...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Entuit Secure Gastrointestinal Suture Anchor Set Recalled by Cook Inc. Due...
The Issue: There is a potential for difficulty in sliding down the retention mechanism...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stingray" Guidewire Recalled by Boston Scientific Corporation Due to A batch...
The Issue: A batch of 185cm Stingray Guidewires are incorrectly labeled as 300cm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hemotherm CE Dual Reservoir Cooler/Heater Recalled by Cincinnati Sub-Zero...
The Issue: Evidence supports that when customers performed a fuse replacement as part...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity TF PET/CT (non-RoHS) Recalled by Philips Medical Systems...
The Issue: A software update is being issued to correct multiple issues identified in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cochlear Baha 5 Sound Processor Tamper Proof Battery Door (3 pcs.) Recalled...
The Issue: Product was packaged with the Incorrect tamper proof battery door.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Omnipod DASH Insulin Management System Recalled by Insulet Corporation Due...
The Issue: There is a potential for a communication interruption following a bolus...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aguja de Aspiracion con Profundidad Ajustable Tipo I 16ga x Recalled by...
The Issue: Argon Medical has identified an internal manufacturing issue on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aguja para Biopsia Tipo Medula Osea Ergonomica 11ga x 10cm Recalled by...
The Issue: Argon Medical has identified an internal manufacturing issue on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: J Type Bone Marrow Needle 13ga x 6cm - Product Recalled by Angiotech (Manan...
The Issue: Argon Medical has identified an internal manufacturing issue on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aguja de Aspiration con Profundidad Ajustable Tipo I 15ga x Recalled by...
The Issue: Argon Medical has identified an internal manufacturing issue on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: J Type Bone Marrow Needle 13ga x 10 cm- Product Recalled by Angiotech (Manan...
The Issue: Argon Medical has identified an internal manufacturing issue on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.