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. 2,324 recalls have been distributed to South Dakota in the last 12 months.

47,632 total recalls
2,324 in last 12 months

Showing 3588135900 of 47,632 recalls

DrugJune 8, 2015· Life Science Pharmacy Inc

Recalled Item: METHYLFOLATE Capsules Recalled by Life Science Pharmacy Inc Due to...

The Issue: Penicillin Cross Contamination: potentially contaminated with penicillin

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 8, 2015· Life Science Pharmacy Inc

Recalled Item: BI-EST Suspensions Recalled by Life Science Pharmacy Inc Due to Penicillin...

The Issue: Penicillin Cross Contamination: potentially contaminated with penicillin

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 8, 2015· Life Science Pharmacy Inc

Recalled Item: ESTRIOL Vaginal Gels Recalled by Life Science Pharmacy Inc Due to Penicillin...

The Issue: Penicillin Cross Contamination: potentially contaminated with penicillin

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 8, 2015· Life Science Pharmacy Inc

Recalled Item: BI-EST Lozenges Recalled by Life Science Pharmacy Inc Due to Penicillin...

The Issue: Penicillin Cross Contamination: potentially contaminated with penicillin

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 8, 2015· Life Science Pharmacy Inc

Recalled Item: BI-EST Creams Recalled by Life Science Pharmacy Inc Due to Penicillin Cross...

The Issue: Penicillin Cross Contamination: potentially contaminated with penicillin

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 8, 2015· Life Science Pharmacy Inc

Recalled Item: TRI-EST Gels Recalled by Life Science Pharmacy Inc Due to Penicillin Cross...

The Issue: Penicillin Cross Contamination: potentially contaminated with penicillin

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 8, 2015· Life Science Pharmacy Inc

Recalled Item: ESTRIOL Creams Recalled by Life Science Pharmacy Inc Due to Penicillin Cross...

The Issue: Penicillin Cross Contamination: potentially contaminated with penicillin

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 8, 2015· Life Science Pharmacy Inc

Recalled Item: HYDROXOCOBALAMIN Injection Recalled by Life Science Pharmacy Inc Due to...

The Issue: Penicillin Cross Contamination: potentially contaminated with penicillin

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 8, 2015· Life Science Pharmacy Inc

Recalled Item: BI-EST Capsules Recalled by Life Science Pharmacy Inc Due to Penicillin...

The Issue: Penicillin Cross Contamination: potentially contaminated with penicillin

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 5, 2015· Geritrex Corp

Recalled Item: Carb-O-Philic 40 Cream Recalled by Geritrex Corp Due to CGMP Deviation: Poor...

The Issue: CGMP Deviation: Poor container closure of the bulk storage container

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

Class III — Low RiskOngoing
Refund
Medical DeviceJune 5, 2015· Philips Electronics North America Corporation

Recalled Item: Philips HeartStart XL+ Defibrillator/Monitor Product Usage: The HeartStart...

The Issue: Multiple software and hardware issues with device that can affect its function.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2015· Cochlear Americas Inc.

Recalled Item: Cochlear Nucleus Sterile Silicone Template Product Usage: The Cochlear...

The Issue: Cochlear Americas is recalling Nucleus Sterile Silicone Template...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 4, 2015· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Emotion 6 Recalled by Siemens Medical Solutions USA, Inc Due to A...

The Issue: A potential safety issue involving two (2) broken screws and one (1) bowed,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 4, 2015· Volcano Corporation

Recalled Item: Volcano PV .035 Catheter: Part number: 88901 Recalled by Volcano Corporation...

The Issue: During a relabeling procedure at the manufacturing facility, the products...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 4, 2015· Panoramic Rental Corp.

Recalled Item: Panoramic X-ray Model PC-1000 The PC-1000 will enable the user Recalled by...

The Issue: Jackscrew nut part failure potentially leading to device malfunction and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 4, 2015· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Emotion 16 Recalled by Siemens Medical Solutions USA, Inc Due to A...

The Issue: A potential safety issue involving two (2) broken screws and one (1) bowed,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 4, 2015· Omnilife Science Inc.

Recalled Item: APEX INTERFACE Hemi 54X and Flared 56X Recalled by Omnilife Science Inc. Due...

The Issue: The device may have improper screw hole placement due to inaccurate location...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 4, 2015· Volcano Corporation

Recalled Item: Prestige Plus 185cm J-Tip: Part number: 9185J Recalled by Volcano...

The Issue: During a relabeling procedure at the manufacturing facility, the products...

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

Class II — Potential Health HazardOngoing
DrugJune 4, 2015· Actavis Inc

Recalled Item: Lutera (0.1 mg levonorgestrel and 0.02 mg ethinyl estradiol tablets USP)...

The Issue: Labeling: Incorrect or Missing Package Insert; Product is being recalled...

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

Class III — Low RiskOngoing
Refund
DrugJune 4, 2015· Fresenius Kabi USA, LLC

Recalled Item: Rifampin for Injection Recalled by Fresenius Kabi USA, LLC Due to Failed...

The Issue: Failed Impurities/Degradation Specifications; out-of-specification for...

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

Class II — Potential Health HazardOngoing
Refund