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.

47,632 total recalls
1,734 in last 12 months

Showing 3974139760 of 47,632 recalls

DrugJune 26, 2014· Caraco Pharmaceutical Laboratories, Ltd.

Recalled Item: Cephalexin Capsules Recalled by Caraco Pharmaceutical Laboratories, Ltd. Due...

The Issue: CGMP Deviations: These products are being recalled because they were...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJune 26, 2014· Poly Pharmaceuticals, Inc

Recalled Item: POLY-TUSSIN AC LIQUID Recalled by Poly Pharmaceuticals, Inc Due to Does Not...

The Issue: Does Not Meet Monograph: Phenylephrine and pseudoephedrine are below...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugJune 26, 2014· Poly Pharmaceuticals, Inc

Recalled Item: LORTUSS EX Recalled by Poly Pharmaceuticals, Inc Due to Does Not Meet...

The Issue: Does Not Meet Monograph: Phenylephrine and pseudoephedrine are below...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
Medical DeviceJune 26, 2014· Hill-Rom, Inc.

Recalled Item: Affinity¿ Four Birthing Bed Recalled by Hill-Rom, Inc. Due to The attachment...

The Issue: The attachment latch mechanism can become bent depending on user handling....

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2014· Biosound Esaote, Inc.

Recalled Item: Esaote PA230E Transducer A portable and cart base ultrasound system Recalled...

The Issue: Using the PA230E transducer with a user-defined setting with the output...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2014· Alphatec Spine, Inc.

Recalled Item: Solanas 2.1mm FIXED DEPTH DRILL Recalled by Alphatec Spine, Inc. Due to...

The Issue: Alphatec Spine is recalling the 2.1mm Fixed Depth Drill 10mm because they...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 25, 2014· Zimmer, Inc.

Recalled Item: Zimmer Dental Tapered Screw-Vent Implant Recalled by Zimmer, Inc. Due to...

The Issue: Zimmer Dental is conducting a voluntary recall of a single lot of the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 25, 2014· Mckesson Information Solutions LLC

Recalled Item: McKesson Cardiology Hemo. McKesson Cardiology" Hemo is intended for complete...

The Issue: McKesson Cardiology Hemo front-end parameter boxes must undergo annual...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 25, 2014· Salter Labs

Recalled Item: Oxygen Mask Recalled by Salter Labs Due to The case label correctly states...

The Issue: The case label correctly states partial rebreather but the insert label...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 25, 2014· Peters Surgical

Recalled Item: The synthetic non-absorbable surgical sutures CARDIOFLON Evolution are...

The Issue: A potential splitting of the surface treatment of the thread ends on certain...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 25, 2014· Karl Storz Endoscopy

Recalled Item: Essential NEO Recalled by Karl Storz Endoscopy Due to KARL STORZ...

The Issue: KARL STORZ Endoscopy-America is recalling the Essential NEO because the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 25, 2014· Peters Surgical

Recalled Item: The synthetic non-absorbable surgical sutures CARDIOXYL are composed of a...

The Issue: A potential splitting of the surface treatment of the thread ends on certain...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugJune 25, 2014· Medical Supply Liquidators Llc

Recalled Item: L-Carnitine Injection USP 100 mg/ml Recalled by Medical Supply Liquidators...

The Issue: Marketed without an Approved NDA/ANDA; IM and SQ injectable products are...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJune 25, 2014· Medical Supply Liquidators Llc

Recalled Item: G.A.C. 375 Injection USP Recalled by Medical Supply Liquidators Llc Due to...

The Issue: Marketed without an Approved NDA/ANDA; IM and SQ injectable products are...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJune 25, 2014· Medical Supply Liquidators Llc

Recalled Item: Vitamin B12 Hydroxocobalamin Injection USP 1000 mcg/ml Recalled by Medical...

The Issue: Marketed without an Approved NDA/ANDA; IM and SQ injectable products are...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJune 25, 2014· Medical Supply Liquidators Llc

Recalled Item: BCAA 4% Branched Chain Amino Acid Injection USP Recalled by Medical Supply...

The Issue: Marketed without an Approved NDA/ANDA; IM and SQ injectable products are...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJune 25, 2014· Medical Supply Liquidators Llc

Recalled Item: Glutathione Injection USP Recalled by Medical Supply Liquidators Llc Due to...

The Issue: Marketed without an Approved NDA/ANDA; IM and SQ injectable products are...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJune 25, 2014· Medical Supply Liquidators Llc

Recalled Item: Vitamin B12 Methylcobalamin 5000 Injection USP 5000 mcg/ml Recalled by...

The Issue: Marketed without an Approved NDA/ANDA; IM and SQ injectable products are...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJune 25, 2014· Medical Supply Liquidators Llc

Recalled Item: Super MIC B Complex for L-Carnitine for Injection USP with Recalled by...

The Issue: Marketed without an Approved NDA/ANDA; IM and SQ injectable products are...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJune 25, 2014· Medical Supply Liquidators Llc

Recalled Item: Vitamin B12 Methylcobalamin Injection USP 1000 mcg/ml Recalled by Medical...

The Issue: Marketed without an Approved NDA/ANDA; IM and SQ injectable products are...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund