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 47381–47400 of 47,632 recalls
Recalled Item: Medpro Elastomeric Infusion Pump. AccuFlux Recalled by First Medical Source...
The Issue: Please be aware that this is not a new recall. The firm has taken action;...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pointe Scientific Lactate Dehydrogenase (Liquid) Reagent Set Model...
The Issue: Pointe Scientific Lactate Dehydrogenase (Liquid) Reagent Set stability claim...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Jimmy Peppers Hot Cherry Sliced Peppers Recalled by Cosmo's Food Products,...
The Issue: Product contains foreign material
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Murocel (methylcellulose) Lubricant Opthalmic Solution (USP Recalled by...
The Issue: Lack of Assurance of Sterility: Bausch & Lomb, Inc. is recalling 7 Lots of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sigma Spectrum VOLUMETRIC INFUSION PUMP Recalled by Baxter Healthcare...
The Issue: Recall expansion; the infusion pumps have the potential to fail causing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Daytrana (methylphenidate) transdermal system patch Recalled by Noven...
The Issue: Miscalibrated and/or Defective Delivery System: Out of Specification results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Daytrana (methylphenidate) transdermal system patch Recalled by Noven...
The Issue: Miscalibrated and/or Defective Delivery System: Out of Specification results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Daytrana (methylphenidate) transdermal system patch Recalled by Noven...
The Issue: Miscalibrated and/or Defective Delivery System: Out of Specification results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Daytrana (methylphenidate) transdermal system patch Recalled by Noven...
The Issue: Miscalibrated and/or Defective Delivery System: Out of Specification results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Genesis Straight Esthetic 5.0 mm 3. mm Cuff Abutment Part Recalled by...
The Issue: Mislabeled: Genesis Straight Esthetic 4.0mm Contour ,1mm cuff labeled as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Genesis Straight Esthetic 4.0 mm 1mm Cuff Abutment Part Number: Recalled by...
The Issue: Mislabeled: Genesis Straight Esthetic 5.0mm Contour ,3mm cuff labeled as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Catheter Irrigation Set labeled in part: ***24K Arthroscopy Outflow/Suction...
The Issue: ConMed Linvatec recalled their 24k Arthroscopy Outflow/Suction Tubing Set...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: epoc Blood Analysis BGEM Test Cards for use with the Recalled by Epocal Inc...
The Issue: Customer reported problem while performing incoming QC of newly received lot...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ******eMax 2 Plus Console***SN G 10307653002*** Product Usage: The Recalled...
The Issue: The RPM of the Motor Handpiece may be less than 80,000 RPM.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ******eMax 2 Plus Console Recalled by The Anspach Effort, Inc. Due to The...
The Issue: The RPM of the Motor Handpiece may be less than 80,000 RPM.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ******eMax 2 Plus Console Recalled by The Anspach Effort, Inc. Due to The...
The Issue: The RPM of the Motor Handpiece may be less than 80,000 RPM.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Albuterol Sulfate Inhalation Solution Recalled by Nephron Pharmaceuticals...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Azelastine HCl Nasal Solution Recalled by Apotex Corp. Due to CGMP...
The Issue: CGMP Deviations: tubing used for filling may interact with the nasal...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Z-800 Volumetric Infusion System. For intravenous infusion of parenteral...
The Issue: Update Instruction For Use for Preventative Maintenance (PM) Schedule and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vegi-Fiber Plus Recalled by Wynlife Healthcare, Inc. Due to Wynlife...
The Issue: Wynlife healthcare is recalling their All-In-One Probiotics and Vegi-Fiber...
Recommended Action: Do not consume. Return to store for a refund or discard.