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. 2,349 recalls have been distributed to South Dakota in the last 12 months.
Showing 29561–29580 of 47,632 recalls
Recalled Item: various polyethylene implants BIO PLUG 10MM Product Usage: Non-weight...
The Issue: Endotoxin levels higher than process maximum limits were discovered in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: various polyethylene implants Hips Active Articulation ArComXL Bearings...
The Issue: Endotoxin levels higher than process maximum limits were discovered in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: various polyethylene implants Extremities Recalled by Zimmer Biomet, Inc....
The Issue: Endotoxin levels higher than process maximum limits were discovered in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: various polyethylene implants Custom parts Product Usage: Custom Recalled by...
The Issue: Endotoxin levels higher than process maximum limits were discovered in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: XtraHRD Natural Male Enhancement Capsules Recalled by Organic Herbal Supply...
The Issue: Marketed without an Approved NDA/ANDA: Product contains N-desmethyl...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HealthA2Z CHEWABLE Aspirin (NSAID) 81 mg Recalled by Allegiant Health Due to...
The Issue: cGMP deviations - presence of rubber particles found loose in the bulk product.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 7F Prelude¿ Short Sheath Introducer. Catalog Numbers: K15-00070 Recalled by...
The Issue: Merit Medical Systems, Inc. announces a voluntary field action for sheaths...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ropivacaine HCl 0.2% 400 mL Total Volume in an ON-Q Recalled by Pharmedium...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ropivacaine HCl 0.2% 500 mL Total Volume in an ON-Q Recalled by Pharmedium...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ropivacaine HCl 0.2% 750 mL Total Volume in an ON-Q Recalled by Pharmedium...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ropivacaine HCl 0.2% 500 mL Total Volume in an ON-Q Recalled by Pharmedium...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bupivacaine HCl 0.25% 270 mL Total Volume in an ON-Q Recalled by Pharmedium...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bupivacaine HCl 0.25% 400 mL Total Volume in an ON-Q Recalled by Pharmedium...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ropivacaine HCl 0.2% 550 mL Total Volume in an AutoFuser Recalled by...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Famciclovir tablets Recalled by AVKARE Inc. Due to Failed impurities/...
The Issue: Failed impurities/ degradation specifications: Product was above...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Zenatane (isotretinoin) capsules Recalled by Dr. Reddy's Laboratories, Inc....
The Issue: Failed dissolution specifications - low dissolution results at S3 stage.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Zenatane (isotretinoin) capsules Recalled by Dr. Reddy's Laboratories, Inc....
The Issue: Failed dissolution specifications - low dissolution results at S3 stage.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Zenatane (isotretinoin) capsules Recalled by Dr. Reddy's Laboratories, Inc....
The Issue: Failed dissolution specifications - low dissolution results at S3 stage.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Zenatane (isotretinoin) capsules Recalled by Dr. Reddy's Laboratories, Inc....
The Issue: Failed dissolution specifications - low dissolution results at S3 stage.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Miriam Capsule Endoscope System. Model MR1100 Product Usage: MiroCam Capsule...
The Issue: When a user switches on MR1100 Receiver, even though the battery was fully...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.