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. 2,259 recalls have been distributed to South Dakota in the last 12 months.
Showing 46001–46020 of 47,632 recalls
Recalled Item: Universal Flex2 Breathing Circuit Class I 510(k) Exempt An anesthesia...
The Issue: King Systems received a customer complaint indicating that the customer had...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optilock 2.7 mm Screw Inserter. Intended Use: The OptiLock Upper Recalled by...
The Issue: Field complaints indicate that recent shipments of the 14-400795 and 36505...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optilock T15 AO Driver (3.5mm). Intended Use: The OptiLock Upper Recalled by...
The Issue: Field complaints indicate that recent shipments of the 14-400795 and 36505...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dual Tip Marker Recalled by Viscot Medical LLC Due to Dual Tip Marker has...
The Issue: Dual Tip Marker has inconsistent ink flow on the black permanent ink side.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: S-Lift Implant Guides (also known as S-LIF) Compressor Part Number: Recalled...
The Issue: When using the optional S-LIFT (also known as S-LIF) Implant Guides without...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: S-Rom¿ Total Hip System Poly Liner Packaging: The insert is Recalled by...
The Issue: Orthopaedics, Inc. (DePuy) is issuing a voluntary recall of four lots of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 12/14 TAPER HIGH OFFSET NECK USE WITH SMITH & NEPHEW Recalled by Smith &...
The Issue: Modular necks were manufactured out of specification by a vendor; the taper...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atorvastatin Calcium Tablets Recalled by Ranbaxy Inc. Due to Adulterated...
The Issue: Adulterated Presence of Foreign Tablets: A product complaint was received by...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Organic Pine Nuts (Raw Recalled by Newark Nut Stores, Inc. Due to Pine nuts...
The Issue: Pine nuts may contain peanuts
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Furikake (a Japanese rice seasoning of seaweed flakes with...
The Issue: The firm recalled the product due to undeclared eggs, soybeans, and wheat....
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Original Snaps Classic Chewy Candy Recalled by American Licorice Co Due to...
The Issue: CA Dept. of Public Health collected random samples of Red Vines Black...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: RED VINES Mixed Bites Recalled by American Licorice Co Due to CA Dept. of...
The Issue: CA Dept. of Public Health collected random samples of Red Vines Black...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Red Vines Black Licorice Twists Recalled by American Licorice Co Due to CA...
The Issue: CA Dept. of Public Health collected random samples of Red Vines Black...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Oxoid Antimicrobial Susceptibility Discs Recalled by Remel Inc Due to The...
The Issue: The firm is recalling the product because the cartridges may contain discs...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oxoid Antimicrobial Susceptibility Test Discs Recalled by Remel Inc Due to...
The Issue: The firm is recalling the product due to some cartridges may contain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vycor Medical ViewSite Brain Access System 17mm/ 11mm / 5cm Recalled by...
The Issue: Vycor Medical recalled their VBAS (Vycor Viewsite Brain Access System)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ETHICON SURGIFLO HEMOSTATIC MATRIX KIT Plus FlexTip with Thrombin...
The Issue: SURGIFLO Hemostatic Matrix Kit & SURGIFLO Hemostatic Matrix Kit with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ETHICON SURGIFLO HEMOSTATIC MATRIX Distributed by ETHICON ETHICON Recalled...
The Issue: SURGIFLO Hemostatic Matrix Kit & SURGIFLO Hemostatic Matrix Kit with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oncentra External Beam 4.1. Radiation treatment planning software designed...
The Issue: During the planning process the beam weights can be changed by the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Mobilett Mira. Mobile X-Ray System. Recalled by Siemens Medical...
The Issue: During regular product monitoring, Siemens has become aware of a potential...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.