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.

47,632 total recalls
2,339 in last 12 months

Showing 3334133360 of 47,632 recalls

Medical DeviceFebruary 10, 2016· Arrow International, Inc., Division of Teleflex Medical Inc.

Recalled Item: UltraFlex IAB: 7.5Fr 30cc Recalled by Arrow International, Inc., Division of...

The Issue: The sheath body may become separated from the sheath hub. If the separation...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 10, 2016· Arrow International, Inc., Division of Teleflex Medical Inc.

Recalled Item: RediGuard IAB: 7Fr 30cc Recalled by Arrow International, Inc., Division of...

The Issue: The sheath body may become separated from the sheath hub. If the separation...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 9, 2016· Bard Peripheral Vascular Inc

Recalled Item: Denali Filter-Jugular/Subclavian Delivery System Product Code: DL900J/DL950J...

The Issue: Bard Peripheral Vascular, Inc. is recalling Denali Filter-Jugular/Subclavian...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 9, 2016· Merge Healthcare, Inc.

Recalled Item: Merge Cardio software. The firm name on the label is Merge Healthcare...

The Issue: A report can be confirmed with the incorrect patient demographics resulting...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 9, 2016· Bard Peripheral Vascular Inc

Recalled Item: Denali Filter-Femoral Delivery System Product Code: DL900F/DL950F Recalled...

The Issue: Bard Peripheral Vascular, Inc. is recalling Denali Filter-Jugular/Subclavian...

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

Class II — Potential Health HazardOngoing
DrugFebruary 9, 2016· Alcon Research, Ltd.

Recalled Item: TEARS Naturale FREE (dextran 70 and hypromellose 2910) lubricant eye drops...

The Issue: Lack of Assurance of Sterility: Some single-use vials may be filled with...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 8, 2016· Keystone Laboratories Inc

Recalled Item: Medicated Better Braids Recalled by Keystone Laboratories Inc Due to...

The Issue: Microbial Contamination of a Non-Sterile Products: The product had a...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 8, 2016· MicroAire Surgical Instruments, LLC

Recalled Item: MicroAire PAL-R4011XL - 40cm x 4 mm Del Vecchio French Rasp aspiration...

The Issue: Complaints that the cannula bent/broke during surgery.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2016· Ormco/Sybronendo

Recalled Item: TF Adaptive Gutta Percha Point Size SM3 50pk Recalled by Ormco/Sybronendo...

The Issue: Ormco Corporation is recalling the TF Adaptive Gutta Percha Point Size...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2016· MicroAire Surgical Instruments, LLC

Recalled Item: MicroAire PAL¿ Cannula Product Usage - Power Aspiration Device Recalled by...

The Issue: MicroAire has initiated a recall on product PAL-R4011XL (40cm x 4mm Del...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2016· Volcano Corporation

Recalled Item: Volcano R100 Sterile Equipment Cover Recalled by Volcano Corporation Due to...

The Issue: Volcano Corporation has identified that certain lot numbers of Volcano R-100...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2016· Volcano Corporation

Recalled Item: Volcano SpinVision Sterile Equip cover II Recalled by Volcano Corporation...

The Issue: Volcano Corporation has identified that certain lot numbers of Volcano R-100...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2016· Beckman Coulter Inc.

Recalled Item: Allegra X-5 rotor yoke Recalled by Beckman Coulter Inc. Due to A defective...

The Issue: A defective rotor yoke on Allegra X-5 allows improper rotor seating on the...

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

Class II — Potential Health HazardOngoing
DrugFebruary 5, 2016· Baxter Healthcare Corp.

Recalled Item: 0.9% Sodium Chloride Irrigation Recalled by Baxter Healthcare Corp. Due to...

The Issue: PRESENCE OF PARTICULATE MATTER: Product complaint for the presence of...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 5, 2016· AstraZeneca Pharmaceuticals LP

Recalled Item: Tudorza Pressair (aclindinium bromide inhalation powder) Recalled by...

The Issue: Defective Delivery System: Some units have actuation counters set to a...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 5, 2016· Teva Pharmaceuticals USA

Recalled Item: Paricalcitol Capsules Recalled by Teva Pharmaceuticals USA Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: Out of specification test...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 4, 2016· Hartley Medical Center Pharmacy, Incorporated

Recalled Item: Morphine Sulfate 50 mg/ml/Bupivacaine HCL 24 mg/ml Recalled by Hartley...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 4, 2016· Hartley Medical Center Pharmacy, Incorporated

Recalled Item: Fentanyl Citrate 1.275 mg/ml/Baclofen 150 mcg/ml/Bupivacaine HCL 20 mg/ml/...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 4, 2016· Hartley Medical Center Pharmacy, Incorporated

Recalled Item: Hydromorphone HCL 25 mg/ml/Bupivacaine HCL 4 mg/ml Recalled by Hartley...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 4, 2016· Hartley Medical Center Pharmacy, Incorporated

Recalled Item: Hydromorphone HCL 10 mg/ml Recalled by Hartley Medical Center Pharmacy,...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund