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. 2,339 recalls have been distributed to South Dakota in the last 12 months.
Showing 33121–33140 of 47,632 recalls
Recalled Item: Dextrose Injection Recalled by Hospira Inc. Due to Chemical Contamination:...
The Issue: Chemical Contamination: Potential for contamination of the products with an...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dextrose Injection Recalled by Hospira Inc. Due to Chemical Contamination:...
The Issue: Chemical Contamination: Potential for contamination of the products with an...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Potassium Chloride Injection 20 mEq Recalled by Hospira Inc. Due to Chemical...
The Issue: Chemical Contamination: Potential for contamination of the products with an...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Mannitol I.V. Recalled by Hospira Inc. Due to Chemical Contamination:...
The Issue: Chemical Contamination: Potential for contamination of the products with an...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Diana Automated Compounding System Recalled by ICU Medical, Inc. Due to ICU...
The Issue: ICU Medical Inc. has received a report of compounded volumes not meeting the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diana Automated Compounding System Recalled by ICU Medical, Inc. Due to ICU...
The Issue: ICU Medical Inc. has received a report of compounded volumes not meeting the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Liko Universal SlingBars Universal SlingBar" 350 Recalled by Hill-Rom, Inc....
The Issue: The center bolt of the sling bar, which connects the bar to the patient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diana Automated Compounding System Recalled by ICU Medical, Inc. Due to ICU...
The Issue: ICU Medical Inc. has received a report of compounded volumes not meeting the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Helios HL3T and HLT Track Mounted Dental Lights Product Usage: Recalled by...
The Issue: The firm received two customer complaints local Pelton & Crane distributors...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diana Automated Compounding System Recalled by ICU Medical, Inc. Due to ICU...
The Issue: ICU Medical Inc. has received a report of compounded volumes not meeting the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diana Automated Compounding System Recalled by ICU Medical, Inc. Due to ICU...
The Issue: ICU Medical Inc. has received a report of compounded volumes not meeting the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diana Automated Compounding System Recalled by ICU Medical, Inc. Due to ICU...
The Issue: ICU Medical Inc. has received a report of compounded volumes not meeting the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VERO MHI-TM2000 Linear Accelerator System --- Common Name: Medical Linear...
The Issue: In rare cases the VERO/MHI-TM2000 Operator Console could set an incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Estradiol III Recalled by Roche Diagnostics Operations, Inc. Due to Due to...
The Issue: Due to the risk of a recently identified cross reactivity, the Elecsys...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Estradiol II Elecsys and cobas e analyzers 190 Recalled by Roche Diagnostics...
The Issue: Due to the risk of a recently identified cross reactivity, the Elecsys...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Spectra-System Dental Implant 2008 system is comprised of dental...
The Issue: Implant Direct Sybron Manufacturing, LLC is recalling GoDirect Implants...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BARD ArcticGel Pads Product Usage: The Arctic Sun Temperature Management...
The Issue: Complaints were received of restricted/inaccurate flow rate.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Guardian II Hemostasis Valve Recalled by Vascular Solutions, Inc. Due to...
The Issue: Vascular Solutions became aware of a potential problem with the click...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GoGo squeeZ Recalled by Materne North America Corp Due to Materne North...
The Issue: Materne North America Corp. is voluntarily recalling specific packages of...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: GoGo squeeZ Recalled by Materne North America Corp Due to Materne North...
The Issue: Materne North America Corp. is voluntarily recalling specific packages of...
Recommended Action: Do not consume. Return to store for a refund or discard.