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 45861–45880 of 47,632 recalls
Recalled Item: materials "RETINAL OCT Analysis and Interpretation Method" shipped with...
The Issue: Devices labeled for an intended use not included in the existing 510(k) or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Clearlink System Buretrol Solution Set Recalled by Baxter Healthcare...
The Issue: Baxter has determined that the ball-valve feature of the Buretrol Solution...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Interlink System Buretrol Solution Set Recalled by Baxter Healthcare...
The Issue: Baxter has determined that the ball-valve feature of the Buretrol Solution...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Clearlink System Buretrol Solution Set Recalled by Baxter Healthcare...
The Issue: Baxter has determined that the ball-valve feature of the Buretrol Solution...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Interlink System Buretrol Solution Set with 150 mL Burette Recalled...
The Issue: Baxter has determined that the ball-valve feature of the Buretrol Solution...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8 Fr. Bardex Pediatric All-Silicone Foley Catheter with a 3cc Recalled by...
The Issue: The 8 Fr. Bardex All-Silicone Foley Catheter with 3cc balloon had an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cemented Tibial Drill Product Usage: The cemented tibial drill is Recalled...
The Issue: Zimmer is initiating a recall of the Cemented Tibial Drill for the Zimmer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Orajel Kids My Way! Anticavity Fluoride (sodium fluoride) toothpaste...
The Issue: CGMP Deviations: Product was made with an incorrect ingredient, Laureth-9...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: florAlign Prebiotic Formula Recalled by Eco Health, Inc. Due to Potential...
The Issue: Eco Health is recalling florAlign Prebiotic Formula because it has the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: 3/16" Slivered Red Onions Recalled by Gills Onions, LLC Due to Potential...
The Issue: Gills Onions is recalling diced and slivered onions because it may be...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: 1/4" Diced Red Onions Recalled by Gills Onions, LLC Due to Potential...
The Issue: Gills Onions is recalling diced and slivered onions because it may be...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: 1/4" Slivered Yellow Onions Recalled by Gills Onions, LLC Due to Potential...
The Issue: Gills Onions is recalling diced and slivered onions because it may be...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: 1/2" Diced Yellow Onions Recalled by Gills Onions, LLC Due to Potential...
The Issue: Gills Onions is recalling diced and slivered onions because it may be...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: SpiraLok 6.5mm with Ethibond and needles Product Number: 222962 SPIRALOK...
The Issue: Fracture of SPIRALOK Anchors post op, requiring patient revision
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SpiraLok 6.5mm with Ethibond without needles Product Number: 222966 SPIRALOK...
The Issue: Fracture of SPIRALOK Anchors post op, requiring patient revision
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SpiraLok 5.0 w/out Needles with violet and blue Orthocord Product Recalled...
The Issue: Fracture of SPIRALOK Anchors post op, requiring patient revision
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SpiraLok 5.0mm with Ethibond without needles Product Number: 222964 SPIRALOK...
The Issue: Fracture of SPIRALOK Anchors post op, requiring patient revision
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SpiraLok 6.5 w/Needles with Orthocord Product Number: 222970 SPIRALOK...
The Issue: Fracture of SPIRALOK Anchors post op, requiring patient revision
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SpiraLok 6.5 w/out Needles with Orthocord Product Number: 222971 SPIRALOK...
The Issue: Fracture of SPIRALOK Anchors post op, requiring patient revision
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SpiraLok 6.5 w/out Needles with violet and blue Orthocord Product Recalled...
The Issue: Fracture of SPIRALOK Anchors post op, requiring patient revision
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.