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. 920 recalls have been distributed to South Dakota in the last 12 months.

47,632 total recalls
920 in last 12 months

Showing 42701–42720 of 47,632 recalls

DrugAugust 8, 2013· Novartis Pharmaceuticals Corp.

Recalled Item: Tekturna HCT (aliskiren and hydrochlorothiazide) Tablets 300/25 mg Recalled...

The Issue: Chemical Contamination: Novartis Pharmaceuticals Corporation has recalled...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 8, 2013· Novartis Pharmaceuticals Corp.

Recalled Item: Exforge (amlodipine and valsartan Tablets) 5/320 mg Recalled by Novartis...

The Issue: Chemical Contamination: Novartis Pharmaceuticals Corporation has recalled...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 8, 2013· Novartis Pharmaceuticals Corp.

Recalled Item: Exforge (amlodipine and valsartan Tablets) 5/160 mg Recalled by Novartis...

The Issue: Chemical Contamination: Novartis Pharmaceuticals Corporation has recalled...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 8, 2013· Novartis Pharmaceuticals Corp.

Recalled Item: Stalevo (carbidopa Recalled by Novartis Pharmaceuticals Corp. Due to...

The Issue: Chemical Contamination: Novartis Pharmaceuticals Corporation has recalled...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 7, 2013· Sandoz Incorporated

Recalled Item: Introvale (levonorgestrel and ethinyl estradiol) tablets Recalled by Sandoz...

The Issue: Contraceptive tablets out of sequence: Contraceptive tablets out of...

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

Class III — Low RiskOngoing
Refund
Medical DeviceAugust 7, 2013· Enhancement Medical, LLC

Recalled Item: Enhancement Medical expression. model # EXP-150. Injectable Gel 1.5cc...

The Issue: Manufacturer made a change in the production process that resulted in a...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 7, 2013· Philips Medical Systems (Cleveland) Inc

Recalled Item: Philips MR Systems: Asset 0.5T Recalled by Philips Medical Systems...

The Issue: There is a potential for water to collect in the vent pipe elbow in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2013· GE Healthcare, LLC

Recalled Item: GE Ultrasound ViewPoint 6. Product Usage: ViewPoint is intended to Recalled...

The Issue: GE has recently become aware of a potential safety issue due to the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2013· Smith & Nephew, Inc. Endoscopy Division

Recalled Item: OSTOSTEORAPTOR 2.9 mm Suture Anchor with 1 ULTRABRAID COBRAID Suture...

The Issue: Pinholes detected in a small number of primary pouches that may constitute a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2013· Smith & Nephew, Inc. Endoscopy Division

Recalled Item: TWINFIX Ultra 5.5 mm PLLA-HA Suture Anchor with two #2 ULTRABRAID Sutures...

The Issue: Pinholes detected in a small number of primary pouches that may constitute a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2013· Smith & Nephew, Inc. Endoscopy Division

Recalled Item: OSTEORAPTOR 2.3 mm Suture Anchor with 1 ULTRABRAID COBRAID Suture Recalled...

The Issue: Pinholes detected in a small number of primary pouches that may constitute a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2013· Smith & Nephew, Inc. Endoscopy Division

Recalled Item: BIORAPTOR 2.9 mm Suture Anchor with 2 ULTRABRAID Suture Recalled by Smith &...

The Issue: Pinholes detected in a small number of primary pouches that may constitute a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2013· Smith & Nephew, Inc. Endoscopy Division

Recalled Item: TWINFIX Ultra HA 4.5 mm Suture Anchor with 2 ULTRABRAID Suture Recalled by...

The Issue: Pinholes detected in a small number of primary pouches that may constitute a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2013· Smith & Nephew, Inc. Endoscopy Division

Recalled Item: OSTEORAPTOR 2.9 mm Suture Anchor with 1 ULTRABRAID Suture Recalled by Smith...

The Issue: Pinholes detected in a small number of primary pouches that may constitute a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2013· Smith & Nephew, Inc. Endoscopy Division

Recalled Item: RAPTORMITE" 3.7 mm PLLA with two ULTRABRAID" Sutures Size 0 and Needles...

The Issue: Pinholes detected in a small number of primary pouches that may constitute a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2013· Smith & Nephew, Inc. Endoscopy Division

Recalled Item: OSTEORAPTOR 2.3 mm Suture Anchor with ULTRABRAID COBRAID Suture Recalled by...

The Issue: Pinholes detected in a small number of primary pouches that may constitute a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2013· Smith & Nephew, Inc. Endoscopy Division

Recalled Item: TWINFIX Ultra HA 6.5 mm with 2 ULTRABRAID Suture Recalled by Smith & Nephew,...

The Issue: Pinholes detected in a small number of primary pouches that may constitute a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2013· Smith & Nephew, Inc. Endoscopy Division

Recalled Item: BIORAPTOR 2.9 mm Suture Anchor with DURABRAID" Suture Recalled by Smith &...

The Issue: Pinholes detected in a small number of primary pouches that may constitute a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2013· Smith & Nephew, Inc. Endoscopy Division

Recalled Item: TWINFIX Ultra PLLA/HA 6.5 mm with 3 ULTRABRAID Suture Recalled by Smith &...

The Issue: Pinholes detected in a small number of primary pouches that may constitute a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2013· Smith & Nephew, Inc. Endoscopy Division

Recalled Item: BIORAPTOR 2.9 mm Suture Anchor Recalled by Smith & Nephew, Inc. Endoscopy...

The Issue: Pinholes detected in a small number of primary pouches that may constitute a...

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

Class II — Potential Health HazardOngoing