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. 1,030 recalls have been distributed to South Dakota in the last 12 months.
Showing 15441–15460 of 47,632 recalls
Recalled Item: NovoLog FlexPen (insulin aspart) Injection Recalled by Novo Nordisk Inc Due...
The Issue: Temperature Abuse: product samples were stored at temperatures below 32* F...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Saxenda (liraglutide) Injection Recalled by Novo Nordisk Inc Due to...
The Issue: Temperature Abuse: product samples were stored at temperatures below 32* F...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fiasp FlexTouch (insulin aspart injection) 100 units/mL (U-100) Recalled by...
The Issue: Temperature Abuse: product samples were stored at temperatures below 32* F...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: NovoLog (Insulin aspart) Injection Recalled by Novo Nordisk Inc Due to...
The Issue: Temperature Abuse: product samples were stored at temperatures below 32* F...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bobo's Maple Pecan Oat Bars Recalled by Simply Delicious Inc. Due to Two...
The Issue: Two consumer complaints were received for peanuts in maple pecan bars.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: 365 Whole Foods Market Farm Raised Cooked Shrimp 2 lbs/Ready- Recalled by...
The Issue: One lot of uncooked shrimp was inadvertently packaged as cooked shrimp.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Protek Solo Venous Dilator Set: dilator Recalled by Cardiac Assist, Inc Due...
The Issue: On 02/26/2021, it was found that there were incorrectly packaged Dilator...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Chromosome X Alpha-Satellite in FITC Spectrum - Product Usage: Analyte...
The Issue: Users may observe additional locus specific signals at 9q34. The device pack...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Univation X System knee implant devices as follows: Catalog/Product: NL476...
The Issue: Malfunction- loosening of the implant resulting in a potential revision surgery
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Univation X System Tray Sysem knee implant devices as follows: Recalled by...
The Issue: Malfunction- loosening of the implant resulting in a potential revision surgery
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Univation X System knee implant devices as follows: Catalog/Product: NL488...
The Issue: Malfunction- loosening of the implant resulting in a potential revision surgery
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Univation X System knee implant devices as follows: Catalog/Product: NL482...
The Issue: Malfunction- loosening of the implant resulting in a potential revision surgery
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spectrum IQ - Infusion Pump - Product Usage: intended to Recalled by Baxter...
The Issue: Potentially defective component in the AC power adapter which may fail over...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Univation X System knee implant devices as follows: Catalog/Product: NO156Z...
The Issue: Malfunction- loosening of the implant resulting in a potential revision surgery
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Univation X System knee implant devices as follows: Catalog/Product: NL470...
The Issue: Malfunction- loosening of the implant resulting in a potential revision surgery
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Revolution CT Recalled by GE Healthcare, LLC Due to GE Healthcare has become...
The Issue: GE Healthcare has become aware of a potential issue on the Revolution CT...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centricity Universal Viewer - Product Usage: intended to assist in the...
The Issue: When the Cross Enterprise Display option is enabled on the Centricity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Univation X System knee implant devices as follows: Catalog/Product: NO180Z...
The Issue: Malfunction- loosening of the implant resulting in a potential revision surgery
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Univation X System knee implant devices as follows: Catalog/Product: NL494...
The Issue: Malfunction- loosening of the implant resulting in a potential revision surgery
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Interventional Fluoroscopic X-Ray System ARTIS icono biplane- 11327600 ARTIS...
The Issue: Siemens has become aware of a potential issue with software version VE20C....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.