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. 2,516 recalls have been distributed to South Dakota in the last 12 months.
Showing 9141–9160 of 47,632 recalls
Recalled Item: Midazolam Injection Recalled by Akorn, Inc. Due to CGMP Deviations: Firm...
The Issue: CGMP Deviations: Firm went out of business and could no longer continue...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Calcipotriene Topical Solution Recalled by Akorn, Inc. Due to CGMP...
The Issue: CGMP Deviations: Firm went out of business and could no longer continue...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Timolol Maleate Ophthalmic Solution Recalled by Akorn, Inc. Due to CGMP...
The Issue: CGMP Deviations: Firm went out of business and could no longer continue...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Calcitonin Salmon (synthetic origin) Nasal Spray Recalled by Apotex Corp....
The Issue: Presence of Foreign Substance: Glass splinter particle entrapped inside the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: DYNAMITE SUPER capsule Recalled by Gadget Island, Inc Due to Undeclared...
The Issue: Marketed without an Approved NDA/ANDA: FDA analysis found product to be...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Pro Power Knight Plus capsule Recalled by Gadget Island, Inc Due to...
The Issue: Marketed without an Approved NDA/ANDA: FDA analysis found product to be...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: NUX Male Enhancement capsule Recalled by Gadget Island, Inc Due to...
The Issue: Marketed without an Approved NDA/ANDA: FDA analysis found product to be...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HeartSine Recalled by HeartSine Technologies Ltd Due to Single use battery...
The Issue: Single use battery and electrode cartridge may be rendered inoperable due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FILMARRAY Gastrointestinal (GI) Panel (Part No.: RFIT-ASY-0104 &...
The Issue: The firm has identified an increased risk of obtaining false positive...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Incisive CT for Brazil SKD-Computed Tomography X-Ray System Model: 728146...
The Issue: Metal mounting box on the rotating scanner on rotor (heat exchanger box)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Incisive CT-Computed Tomography X-Ray System Model: 728143 Recalled by...
The Issue: Metal mounting box on the rotating scanner on rotor (heat exchanger box)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Incisive CT Power (China)-Computed Tomography X-Ray System Model: 728148...
The Issue: Metal mounting box on the rotating scanner on rotor (heat exchanger box)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Incisive CT Plus-Computed Tomography X-Ray System Model: 728149 Recalled by...
The Issue: Metal mounting box on the rotating scanner on rotor (heat exchanger box)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ventralight ST w Echo PS 4.5" Circle A low profile Recalled by Davol, Inc....
The Issue: Balloon may not inflate as intended. If the balloon does not inflate during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ventralight ST w EchoPS 4"x6" Ellipse- A low profile Recalled by Davol, Inc....
The Issue: Balloon may not inflate as intended. If the balloon does not inflate during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ventralight ST 4.5" Circle with Echo PS- A low profile Recalled by Davol,...
The Issue: Balloon may not inflate as intended. If the balloon does not inflate during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ventralight ST 4" x 6" Ellipse with Echo PS Catalog Number: 5955460 Recalled...
The Issue: Balloon may not inflate as intended. If the balloon does not inflate during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SteriPack Sterile Polyester Spun Swabs (25 units/Pack)- Intended for sample...
The Issue: Fails Post-Sterilization Sterile Swabs Cantilever (Bend) Testing and may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LINK SymphoKnee System L-Shaped Femoral Augment Recalled by Linkbio Corp....
The Issue: Contains the incorrect implant in the packaging. The packaging incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gabapentin Tablets Recalled by The Harvard Drug Group Due to Product mixup:...
The Issue: Product mixup: one foreign tablet found in product.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.