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. 1,663 recalls have been distributed to South Dakota in the last 12 months.

47,632 total recalls
1,663 in last 12 months

Showing 4416144180 of 47,632 recalls

DrugApril 22, 2013· Nora Apothecary and Alternative Therapies, Inc.

Recalled Item: Methylcobalamin Inj 25mg/ml Syr: 8x0.06mlsyr Recalled by Nora Apothecary and...

The Issue: Lack of Assurance of Sterility: FDA inspection findings resulted in concerns...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 22, 2013· Nora Apothecary and Alternative Therapies, Inc.

Recalled Item: Lidocaine 2% Inj MDV Recalled by Nora Apothecary and Alternative Therapies,...

The Issue: Lack of Assurance of Sterility: FDA inspection findings resulted in concerns...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 22, 2013· Nora Apothecary and Alternative Therapies, Inc.

Recalled Item: Meperidine 100mg/ml MDV Recalled by Nora Apothecary and Alternative...

The Issue: Lack of Assurance of Sterility: FDA inspection findings resulted in concerns...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 22, 2013· Nora Apothecary and Alternative Therapies, Inc.

Recalled Item: Bimix Inj 30:1 MDV: 5ml Recalled by Nora Apothecary and Alternative...

The Issue: Lack of Assurance of Sterility: FDA inspection findings resulted in concerns...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 22, 2013· Siemens Healthcare Diagnostics, Inc.

Recalled Item: HbA1c Flex(R) reagent cartridge (K3105A Recalled by Siemens Healthcare...

The Issue: Positive bias on the lots listed compared to alternate methods and a higher...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2013· Carefusion 2200 Inc

Recalled Item: 1) Adult Manual Resuscitator Recalled by Carefusion 2200 Inc Due to...

The Issue: CareFusion has received four (4) customer reports of a component (oxygen...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2013· Siemens Healthcare Diagnostics, Inc.

Recalled Item: HB1C Flex(R) Reagent Cartridge (DF105A Recalled by Siemens Healthcare...

The Issue: Positive bias on the lots listed compared to alternate methods and a higher...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 19, 2013· Ge Healthcare It

Recalled Item: Centricity Enterprise Archive is a software product for receiving Recalled...

The Issue: GE Healthcare has become aware of a potential data loss issue associated...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 19, 2013· OrthoPediatrics Corp

Recalled Item: 90 Degree Cannulated Infant Blade Plate 35mm x 5mm x Recalled by...

The Issue: Post Market Surveillance of the 90 degree Cannulated Infant Blade Plate...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 19, 2013· OrthoPediatrics Corp

Recalled Item: 90 Degree Cannulated Infant Blade Plate 25mm x 5mm x Recalled by...

The Issue: Post Market Surveillance of the 90 degree Cannulated Infant Blade Plate...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 19, 2013· OrthoPediatrics Corp

Recalled Item: 90 Degree Cannulated Infant Blade Plate 30mm x 5mm x Recalled by...

The Issue: Post Market Surveillance of the 90 degree Cannulated Infant Blade Plate...

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

Class II — Potential Health HazardOngoing
DrugApril 19, 2013· Novartis Consumer Health

Recalled Item: Lamisil AT (terbinafine hydrochloride cream 1% antifungal) Recalled by...

The Issue: Labeling: Incorrect or Missing Lot and/or Expiration date; The Lot and/or...

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

Class III — Low RiskOngoing
Refund
DrugApril 19, 2013· Qualitest Pharmaceuticals

Recalled Item: GLIMEPIRIDE TABLETS USP Recalled by Qualitest Pharmaceuticals Due to Failed...

The Issue: Failed Tablet/Capsule Specifications: One oversized tablet was found in a...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 18, 2013· Sandoz Incorporated

Recalled Item: Amoxicillin Capsules USP 500 mg Recalled by Sandoz Incorporated Due to...

The Issue: Presence of Foreign Substance, Sandoz is recalling certain lots of...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 18, 2013· Cook, Inc.

Recalled Item: Zilver PTX Drug-Eluting Peripheral Stent Recalled by Cook, Inc. Due to Cook...

The Issue: Cook Medical has received a small number of complaints related to the...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 18, 2013· Carl Zeiss Meditec, Inc.

Recalled Item: Zeiss brand OPMI Pentero C Recalled by Carl Zeiss Meditec, Inc. Due to Carl...

The Issue: Carl Zeiss Meditec is conducting a field corrective action for its OPMI...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 18, 2013· Cook, Inc.

Recalled Item: Zilver¿ PTX¿ Drug-Eluting Peripheral Stent - 6 mm X 80mm Recalled by Cook,...

The Issue: Cook Medical has received a small number of complaints related to the...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 17, 2013· Alcon Grieshaber AG

Recalled Item: The Constellation Vision System Pneumatic Handpiece. Indicated for both...

The Issue: Alcon is conducting a Medical Device Removal for the Constellation Pneumatic...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2013· Beckman Coulter Inc.

Recalled Item: Synchron LX System(s) and UniCel DxC 600/800 System(s) Lactate Reagent...

The Issue: Beckman Coulter initiated the recall for the Lactate Assay (LACT) Lot...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2013· Bard Peripheral Vascular Inc

Recalled Item: BARD Biopsy Systems UltraClip Dual Trigger breast tissue marker. Intended...

The Issue: Bard Peripheral Vascular (BPV) has confirmed that some devices with the...

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

Class II — Potential Health HazardOngoing