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. 1,090 recalls have been distributed to South Dakota in the last 12 months.
Showing 2061–2080 of 47,632 recalls
Recalled Item: Lisinopril and Hydrochlorothiazide Tablets USP 20mg/12.5mg Recalled by Lupin...
The Issue: Product Mix Up: This product is being recalled because of a complaint...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levothyroxine Sodium Tablets Recalled by ACCORD HEALTHCARE, INC. Due to...
The Issue: Subpotent Drug: Assay below the approved specification
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: New Mexico Pinon Coffee. Dark Pinon Single Serve 10ct. Product Recalled by...
The Issue: Clear coat seal on the lid of the single serve cups did not get applied...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Gabapentin Capsules Recalled by The Harvard Drug Group LLC Due to Defective...
The Issue: Defective container; blister packaging inadequately sealed.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Gabapentin Capsules Recalled by The Harvard Drug Group LLC Due to Defective...
The Issue: Defective container; blister packaging inadequately sealed.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bardex Lubri-Sil I.C. 400-series Temperature Sensing Silver/Hydrogel Coated...
The Issue: Foley catheter may have an obstructed lumen, which may result in an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Osteotec Product Name: Osteotec Silicone Finger Implant...
The Issue: There is the potential that the silicone implant may contain foreign material
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Recalled by Stryker Corporation Due to Due to complaints their is...
The Issue: Due to complaints their is the potential that irrigation solution may leaked...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic CareLink SmartSync Device Manager Recalled by Medtronic, Inc. Due...
The Issue: In prior SmartSync application versions, the Abort button stopped the test...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: JLM Manufacturing Dark Chocolate Nonpareils Recalled by Lipari Foods...
The Issue: Undeclared milk
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Little Remedies¿ Honey Cough 4 FL OZ (118 mL) Recalled by Prestige Brands...
The Issue: contaminated with Bacillus cereus and may be spoiled
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Product Name: Tense-X. Package: 175cc HDPE Bottle. Type: Vegetable Capsule....
The Issue: Products contains Magnesium Salicylate.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Product Name: Total Comfort. Package: 175cc HDPE Bottle. Type: Vegetable...
The Issue: Products contains Magnesium Salicylate.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Product Name: Nutra Calm Package: 175cc HDPE Bottle. Type: Vegetable...
The Issue: Products contains Magnesium Salicylate.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Stryker Recalled by Stryker Corporation Due to Due to complaints their is...
The Issue: Due to complaints their is the potential that irrigation solution may leaked...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic CareLink SmartSync Patient Connector Recalled by Medtronic, Inc....
The Issue: In prior SmartSync application versions, the Abort button stopped the test...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QuickVue: Dipstick Strep A Test: 50T Recalled by Quidel Corporation Due to...
The Issue: Dipstick strep A test has potential for false positive results.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MI Cancer Seek UDI Code: (01)00860008613325(21)H5HJHDSXF MI Cancer Recalled...
The Issue: Due to an incorrect test results provided that indicated the incorrect drug...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD PhaSeal Injector Luer (N30C) Recalled by BD SWITZERLAND SARL Due to...
The Issue: Closed system drug transfer devices were shipped to the U.S. market without...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SafeStar 60A Plus Filter. Bidirectionally breathing system filter. Recalled...
The Issue: Reports of slow increase of CO2-curve when gas sample is taken from the gas...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.