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. 2,311 recalls have been distributed to South Dakota in the last 12 months.
Showing 36961–36980 of 47,632 recalls
Recalled Item: EPINEPHrine HCl 16 mg added to 250 mL 0.9% Sodium Recalled by Pharmedium...
The Issue: Presence of Particulate Matter: The firm produced products using 0.9% Sodium...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: EPINEPHrine HCl 4 mg added to 250 mL 0.9% Sodium Recalled by Pharmedium...
The Issue: Presence of Particulate Matter: The firm produced products using 0.9% Sodium...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fluoxetine Capsules USP Recalled by Teva Pharmaceuticals USA Due to Chemical...
The Issue: Chemical Contamination: Product recalled due to an elevated level of a...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HEPARIN Sodium Injection USP Recalled by Pharmedium Services, LLC Due to...
The Issue: Presence of Particulate Matter: The firm produced products using 0.9% Sodium...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fluoxetine Capsules USP Recalled by Teva Pharmaceuticals USA Due to Chemical...
The Issue: Chemical Contamination: Product recalled due to an elevated level of a...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HEPARIN Sodium Injection USP 25 Recalled by Pharmedium Services, LLC Due to...
The Issue: Presence of Particulate Matter: The firm produced products using 0.9% Sodium...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: EPINEPHrine HCl 1 mg added to 250 mL 0.9% Sodium Recalled by Pharmedium...
The Issue: Presence of Particulate Matter: The firm produced products using 0.9% Sodium...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: oxyTOCIN 15 Units added to 250 mL 5% Dextrose Injection USP Recalled by...
The Issue: Presence of Particulate Matter: The firm produced products using 0.9% Sodium...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ketorolac Tromethamine Inj. USP Recalled by Hospira Inc. Due to Crystallization
The Issue: Crystallization
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Testosterone Cypionate 200 mg/mL in Sesame oil Recalled by Stroheckers Inc...
The Issue: Incorrect Product Formulation: Vials labeled as Testosterone Cypionate 200...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: MONISTAT 1 SIMPLE CURE (Miconazole Nitrate Vaginal Insert) 1200 mg ovule...
The Issue: Marketed without an approved NDA/ANDA: The distributed units of Monistat 1...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: EPIQ 5 Ultrasound System with Pediatric Cardiology option Recalled by...
The Issue: When Epiq 5 Ultrasound System, WITH the Pediatric Cardiology option, is set...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EPIQ 7 Ultrasound System with Pediatric Cardiology option Recalled by...
The Issue: When Epiq 7 Ultrasound System, WITH the Pediatric Cardiology option, is set...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic SynchroMed II Implantable Infusion Pumps Recalled by Medtronic...
The Issue: Medtronic is conducting a recall of a specific subset of Model 8637-20 and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Primus (THE BTE WS30) Recalled by BTE Technologies, Inc. Due to On the...
The Issue: On the Primus that includes the optional Chop / Lift Bar, there is a remote...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Genesis Malleable Penile Prosthesis Recalled by Coloplast Manufacturing US,...
The Issue: Several lots of the 9.5 mm Genesis Malleable Penile Prosthesis were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BARD MAX-CORE Disposable Core Biopsy Instrument Gauge x Length 18g Recalled...
The Issue: The firm is recalling Bard MAX-CORE Disposable Core Biopsy Instrument due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spinal Elements 5.5 x 45MM Mercury lordosed rod. A component Recalled by...
The Issue: Some rods may not meet the appropriate traceability requirements including...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TFN-ADVANCED Proximal Femoral Nailing System (TFNA) Recalled by Synthes,...
The Issue: TFNA nails from certain lots were assembled with a locking mechanism too...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UBERVITA LOSE WEIGHT FAST W700 THERMOGENIC HYPER-METABOLIZER DIETARY...
The Issue: It has come to the attention of Ubervita LLC that a packaging error has...
Recommended Action: Do not consume. Return to store for a refund or discard.