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. 2,260 recalls have been distributed to South Dakota in the last 12 months.

47,632 total recalls
2,260 in last 12 months

Showing 4434144360 of 47,632 recalls

DrugApril 5, 2013· Glenmark Generics Inc., USA

Recalled Item: Glenmark Topiramate Tablets Recalled by Glenmark Generics Inc., USA Due to...

The Issue: Chemical Contamination: Topiramate Tablets is being recalled due to...

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

Class III — Low RiskOngoing
Refund
Medical DeviceApril 5, 2013· Medtox Diagnostics Inc

Recalled Item: PROFILE-V MEDTOXScan Drugs of Abuse Test System. For the rapid Recalled by...

The Issue: Review of validation information and customer complaints which indicated...

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

Class II — Potential Health HazardOngoing
DrugApril 4, 2013· Aaron Industries Inc

Recalled Item: Rite Aid brand Maximum Strength Tussin Cough & Cold Mucus Relief CF Recalled...

The Issue: Presence of Precipitate; white substance confirmed as Guaifenesin, an active...

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

Class III — Low RiskOngoing
Refund
Medical DeviceApril 4, 2013· Remel Inc

Recalled Item: remel RapID Yeast Plus System Recalled by Remel Inc Due to Mislabeling

The Issue: The two reagents supplied in the RapID Yeast Plus System kit (Reagent A and...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 4, 2013· B. Braun Medical, Inc.

Recalled Item: 20mm addEASE(TM) Binary Connector with 17 Ga. Needle for use Recalled by B....

The Issue: Possible solution leakage at the interface of the addEASE(TM) Binary...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 4, 2013· B. Braun Medical, Inc.

Recalled Item: 13mm addEASE(TM) Binary Connector with 17 Ga. Needle for use Recalled by B....

The Issue: Possible solution leakage at the interface of the addEASE(TM) Binary...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 4, 2013· Leica Microsystems, Inc.

Recalled Item: LPC Fine Mesh Cassette for the Leica LPC Printer. Part No: 14060546848...

The Issue: An LPC Fine Mesh Cassette failed to stay closed during processing operations.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 4, 2013· Polymer Technology Systems, Inc.

Recalled Item: PTS PANELS Recalled by Polymer Technology Systems, Inc. Due to Internal...

The Issue: Internal investigation demonstrated under-recovery for glucose when tested...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 4, 2013· Roche Diagnostics Operations, Inc.

Recalled Item: Cobas¿ 8000 modular analyzer series software version 03-01 Recalled by Roche...

The Issue: When using the cobas e 602 module, Diluent Multiassay may be used for...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 4, 2013· Medshape Solutions, INC.

Recalled Item: ExoShape Soft Tissue Fastener 12 mm x 30 mm by Medshape Solutions, INC. Due...

The Issue: Expiration date on the patient label and date on the product carton were not...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 4, 2013· Siemens Medical Solutions USA, Inc

Recalled Item: Software correction applies to customers who use the RT Therapist Recalled...

The Issue: Software update to fix multiple safety related issues.

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

Class II — Potential Health HazardOngoing
DrugApril 3, 2013· Boehringer Ingelheim Roxane Inc

Recalled Item: Oxcarbazepine Oral Suspension Recalled by Boehringer Ingelheim Roxane Inc...

The Issue: Resuspension Problems: Recalled lot did not meet resuspendability requirements.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 3, 2013· GE Healthcare, LLC

Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare has...

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

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 3, 2013· GE Healthcare, LLC

Recalled Item: SOLAR 8000 AND TRANSPORT PRO WITH PATIENT DATA MODULE (Marketed Recalled by...

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

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 3, 2013· GE Healthcare, LLC

Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare has...

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

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 3, 2013· Toshiba American Medical Systems Inc

Recalled Item: TOSHIBA Kalare Diagnostic X-Ray System K110785 Recalled by Toshiba American...

The Issue: Firm initiated recall because when radiographic conditions with the small...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 3, 2013· Ortho-Clinical Diagnostics

Recalled Item: VITROS Immunodiagnostic Products CK-MB Calibrators Recalled by...

The Issue: Internal testing demonstrated that opened-reconstituted VITROS CK-MB...

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

Class III — Low RiskOngoing
DrugApril 2, 2013· Cetylite Industries, Inc.

Recalled Item: Cetacaine Liquid Topical Anesthetic Recalled by Cetylite Industries, Inc....

The Issue: Subpotent Drug: Cetacaine Topical Anesthetic Liquid is being recalled...

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

Class II — Potential Health HazardOngoing
Refund
FoodApril 2, 2013· Chemi- Source Inc, Nutra Pak

Recalled Item: Sprouts Farmers Market Whey Protein Vanilla: 1 lbs Recalled by Chemi- Source...

The Issue: Source of whey ingredient not listed as milk, an allergen. Consumers who...

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

Class II — Potential Health HazardOngoing
Refund
FoodApril 2, 2013· Chemi- Source Inc, Nutra Pak

Recalled Item: All Natural Whey - Natural Flavor 1.89 LBS: Whey Protein Concentrate and...

The Issue: Source of whey ingredient not listed as milk, an allergen. Consumers who...

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

Class II — Potential Health HazardOngoing
Refund