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 3280132820 of 47,632 recalls

DrugApril 7, 2016· Akorn, Inc.

Recalled Item: Good Neighbor Pharmacy PEG-Phen Lubricant Eye Drops (Polyethylene Glycol 400...

The Issue: Presence of Particulate Matter

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 7, 2016· Fresenius Kabi USA, LLC

Recalled Item: Haloperidol Decanoate Injection Recalled by Fresenius Kabi USA, LLC Due to...

The Issue: Failed Impurities/Degradation Specifications: Firm is recalling product due...

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

Class III — Low RiskOngoing
Refund
Medical DeviceApril 6, 2016· Pentax Medical Company

Recalled Item: Duodenoscope Product Usage: Intended to provide optical visualization of and...

The Issue: Pentax Medical Video Processor EPK-i5010 has been shipped with a reusable...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2016· Pentax Medical Company

Recalled Item: Gastroscope Product Usage: Intended to provide optical visualization of and...

The Issue: Pentax Medical Video Processor EPK-i5010 has been shipped with a reusable...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2016· Pentax Medical Company

Recalled Item: Confocal GI Scope Product Usage: Intended to provide optical visualization...

The Issue: Pentax Medical Video Processor EPK-i5010 has been shipped with a reusable...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2016· Ortho-Clinical Diagnostics

Recalled Item: VITROS 5600 Integrated System Recalled by Ortho-Clinical Diagnostics Due to...

The Issue: Ortho Clinical Diagnostics confirmed a software timing anomaly in which the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2016· Pentax Medical Company

Recalled Item: Ultrasound Gastroscope Product Usage: Intended to provide optical...

The Issue: Pentax Medical Video Processor EPK-i5010 has been shipped with a reusable...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2016· Pentax Medical Company

Recalled Item: Signmoidoscope Product Usage: Intended to provide optical visualization of...

The Issue: Pentax Medical Video Processor EPK-i5010 has been shipped with a reusable...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2016· Skytron, Div. The KMW Group, Inc

Recalled Item: EZ Slide Battery/line powered hydraulic table with removable leg section...

The Issue: The potential exists within the identified tables that incorrectly...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2016· Pentax Medical Company

Recalled Item: Colonoscope Product Usage: Intended to provide optical visualization of and...

The Issue: Pentax Medical Video Processor EPK-i5010 has been shipped with a reusable...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2016· Ortho-Clinical Diagnostics

Recalled Item: VITROS 3600 Immunodiagnostic System Recalled by Ortho-Clinical Diagnostics...

The Issue: Ortho Clinical Diagnostics confirmed a software timing anomaly in which the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 5, 2016· Ceg Enterprises Llc

Recalled Item: Germ Terminator Recalled by Ceg Enterprises Llc Due to CEG Enterprises, LLC...

The Issue: CEG Enterprises, LLC is recalling Germ Terminator Toothbrush Sanitizer GT100...

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

Class II — Potential Health HazardOngoing
FoodApril 5, 2016· Empirical Laboratories, Incorporated

Recalled Item: Liposomal Magnesium Nutritional Supplement. 6 FL. OZ (180 ml) The Recalled...

The Issue: Empirical Labs is recalling Liposomal Magnesium because of the potential for...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
DrugApril 5, 2016· Fresenius Kabi USA, LLC

Recalled Item: Cisatracurium Besylate Injection Recalled by Fresenius Kabi USA, LLC Due to...

The Issue: Incorrect/ Undeclared Excipient: Firm is recalling product due to an...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 4, 2016· Lupin Pharmaceuticals Inc.

Recalled Item: Lisinopril & Hydrochlorothiazide Tables Recalled by Lupin Pharmaceuticals...

The Issue: CGMP Deviations: finished products manufactured using active pharmaceutical...

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

Class III — Low RiskOngoing
Refund
Medical DeviceApril 4, 2016· Merge Healthcare, Inc.

Recalled Item: Merge Eye Station Import Utility (ESIU). The firm name on Recalled by Merge...

The Issue: System locks up which may result in potential patient injury or delay in...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 4, 2016· Merge Healthcare, Inc.

Recalled Item: Merge Eye Station and Merge Eye Care PACS. Recalled by Merge Healthcare,...

The Issue: During an antivirus program scan of the Eye Station or Eye Care PACS, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 4, 2016· Merge Healthcare, Inc.

Recalled Item: iConnect Enterprise Archive software. Recalled by Merge Healthcare, Inc. Due...

The Issue: The versions allow images to be stored without pixel data, resulting in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 4, 2016· Merge Healthcare, Inc.

Recalled Item: iConnect Enterprise Archive when used with RadSuite. The firm name Recalled...

The Issue: The software produced a number of "do not route" exceptions, which may...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 4, 2016· Merge Healthcare, Inc.

Recalled Item: iConnect Enterprise Archive (ICEA) software. iConnect Enterprise Archive is...

The Issue: The study is archived but cannot be opened in iConnect Access and cannot...

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

Class II — Potential Health HazardOngoing