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. 1,734 recalls have been distributed to South Dakota in the last 12 months.
Showing 39621–39640 of 47,632 recalls
Recalled Item: Magna-Fx Cannulated Screw Fixation System Bone Screw Fully Threaded Sterile...
The Issue: Zimmer is recalling various trauma screws that failed a leak test due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 6.5 mm Cancellous Screw 32 mm Thread Length Sterile zimmer Recalled by...
The Issue: Zimmer is recalling various trauma screws that failed a leak test due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bulk organic Carob powder (10# ) Recalled by Dancing Star LLC Due to...
The Issue: Product may be contaminated with Salmonella.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Date Flax with Turmeric Chunks of Energy (10# ) Recalled by Dancing Star LLC...
The Issue: Product may be contaminated with Salmonella.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Carob Supergreens Chunks of Energy (10# ) Recalled by Dancing Star LLC Due...
The Issue: Product may be contaminated with Salmonella.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Medtronic MiniMed Guardian Monitor Recalled by Medtronic MiniMed Inc. Due to...
The Issue: Medtronic MiniMed is recalling the Guardian REAL-Time monitors because of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zenith Slide W-I-D-E Long Term Care Bed Recalled by GF Health Products,...
The Issue: The bed head deck may fail to elevate as expected during normal operation....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stago IVD Recalled by Diagnostica Stago, Inc. Due to Diagnostica Stago Inc....
The Issue: Diagnostica Stago Inc. received some customer complaints regarding a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RENASYS EZ/ RENASYS EZ Plus 800 mL canister with Solidifier Recalled by...
The Issue: RENASYS EZ Canisters exhibiting visible evidence of deformation of the inlet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RENASYS EZ/ RENASYS EZ Plus 800 mL canister (w/o CLP) Recalled by Smith &...
The Issue: RENASYS EZ Canisters exhibiting visible evidence of deformation of the inlet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RENASYS EZ/ RENASYS EZ Plus 250 mL canister with Solidifier Recalled by...
The Issue: RENASYS EZ Canisters exhibiting visible evidence of deformation of the inlet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: All sterile products within expiry Recalled by Unique Pharmaceutical, Ltd...
The Issue: Lack of Sterility Assurance: A recent FDA inspection revealed poor aseptic...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: N-Acetyl Cysteine 20% 4 mL Vial Stock Code: 4133 Recalled by Unique...
The Issue: Non-Sterility: One lot of N-Acetyl Cysteine vials tested positive for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Clonidine HCl Injection Recalled by X-Gen Pharmaceuticals Inc. Due to...
The Issue: Labeling: Label Error On Declared Strength: The side label description...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Pedi-Pak Pedi-Syringe Filter 35 mL Monoject Syringe Rx Only Genesis BPS...
The Issue: Genesis BPS is recalling numerous devices since they did not notify the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TomoTherapy Treatment System Recalled by TomoTherapy Incorporated Due to...
The Issue: Accuray is voluntarily recalling TomoTherapy H Series software versions...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pedi-Pak Pedi-Syringe Filter 60 mL Becton Dickinson/Monoject Syringe Rx Only...
The Issue: Genesis BPS is recalling numerous devices since they did not notify the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pedi-Pak Pedi-Syringe Filter 30 mL Becton Dickinson Syringe Rx Only Genesis...
The Issue: Genesis BPS is recalling numerous devices since they did not notify the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tapered-Screw Vent Implant Recalled by Zimmer, Inc. Due to Zimmer Dental is...
The Issue: Zimmer Dental is recalling the Tapered Screw-Vent Implant because the inner...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Radiomat M+ NIF 14 x 17 Recalled by AGFA Healthcare Corp. Due to Some sheets...
The Issue: Some sheets of the medical screen film are fogged.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.