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. 897 recalls have been distributed to South Dakota in the last 12 months.

47,632 total recalls
897 in last 12 months

Showing 46601–46620 of 47,632 recalls

Medical DeviceJune 1, 2012· PSC Industries Inc

Recalled Item: Bayonet Forceps 8.25 (209.6 mm) 0.5mm Tips Recalled by PSC Industries Inc...

The Issue: Firm officials reported to CIN-DO that for this device, in the labeling on...

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

Class II — Potential Health HazardOngoing
DrugJune 1, 2012· Bracco Diagnostics Inc

Recalled Item: CARDIOGEN-82 (Rubidium Rb 82 Generator) Recalled by Bracco Diagnostics Inc...

The Issue: GMP deviation; Sr-82 levels exceeded alert limit specification

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 31, 2012· Bayer HealthCare Pharmaceuticals Inc.

Recalled Item: Leukine sargramostim 5 x 500 mcg/mL vial Recalled by Bayer HealthCare...

The Issue: Impurities/Degradation Products: A confirmed out of specification result for...

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

Class III — Low RiskOngoing
Refund
Medical DeviceMay 31, 2012· Synthes (USA) Products LLC

Recalled Item: Universal Spinal System Lamina Hooks Synthes Medium TI Lamina Hook Recalled...

The Issue: USS Lamina Hooks, Medium, Right are being recalled because the hooks are...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2012· SALTER LABS

Recalled Item: Adult Divided Cannula end tidal C)2 sampling w/male luer-lock connector. 7...

The Issue: A complaint was received, and later verified, that product labeled as...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2012· Abbott Laboratories

Recalled Item: ARCHITECT CA 19-9XR Reagent Kit Recalled by Abbott Laboratories Due to The...

The Issue: The six ARCHITECT CA 19-9XR reagent lots are demonstrating a shift up in...

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

Class II — Potential Health HazardOngoing
FoodMay 30, 2012· Crown Prince Inc

Recalled Item: Canned oysters. Crown Prince Natural Smoked Oysters with Chili Pepper...

The Issue: The product has been prepared, packed, or held under insanitary conditions...

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

Class III — Low RiskOngoing
Refund
FoodMay 30, 2012· Crown Prince Inc

Recalled Item: Canned oysters. Crown Prince Natural Smoked Oysters in Olive Oil Recalled by...

The Issue: The product has been prepared, packed, or held under insanitary conditions...

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

Class III — Low RiskOngoing
Refund
FoodMay 30, 2012· Crown Prince Inc

Recalled Item: Canned oysters. Crown Prince Whole Boiled Oysters Recalled by Crown Prince...

The Issue: The product has been prepared, packed, or held under insanitary conditions...

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

Class III — Low RiskOngoing
Refund
FoodMay 30, 2012· Milky Way Intl Trading Corp

Recalled Item: Polar Whole Boiled Oysters Recalled by Milky Way Intl Trading Corp Due to MW...

The Issue: MW Polar is recalling Polar Whole Boiled Oysters from Korea because the...

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

Class III — Low RiskOngoing
Refund
FoodMay 30, 2012· Crown Prince Inc

Recalled Item: Canned oysters. Crown Prince Whole Boiled Oysters Recalled by Crown Prince...

The Issue: The product has been prepared, packed, or held under insanitary conditions...

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

Class III — Low RiskOngoing
Refund
DrugMay 30, 2012· VistaPharm, Inc.

Recalled Item: Hydrocodone Bitartrate & Acetaminophen Oral Solution 7.5 mg/325 mg per 15 mL...

The Issue: Impurities/Degradation Products: exceeded specification at 3 month stability...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 29, 2012· Alphatec Spine, Inc.

Recalled Item: TRESTLE LUXE¿ Anterior Cervical Plating System Recalled by Alphatec Spine,...

The Issue: On May 9th 2012 Alphatec Spine received a complaint which reported that the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 29, 2012· Clark Laboratories, Inc. (dba,Trinity Biotech USA)

Recalled Item: Trinity Biotech Recalled by Clark Laboratories, Inc. (dba,Trinity Biotech...

The Issue: The Positive Control for the Captia Varicella-Zoster Virus (VZV) IgG Kit has...

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

Class III — Low RiskOngoing
Medical DeviceMay 29, 2012· Siemens Healthcare Diagnostics, Inc.

Recalled Item: EasyLink Informatic System is included with the Dimension Vista System....

The Issue: When using the EasyLink Quality Control Package the system may not perform...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 29, 2012· Mckesson Medical Imaging Group

Recalled Item: Horizon Medical Imaging system. Product Usage: Horizon Medical Imaging is...

The Issue: There is a potential to save reports in RadReport with an Incorrect Final...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 29, 2012· Siemens Healthcare Diagnostics, Inc.

Recalled Item: syngo(R) Lab Data Manager and syngo(R) Lab Process Manager Recalled by...

The Issue: When using the syngo Quality Control package the system may not perform as...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 29, 2012· Alcon Research, LTD.

Recalled Item: This voluntary medical device correction is related to Alcon products...

The Issue: This medical device correction is related to Alcon products that present a...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 29, 2012· Carefusion 2200 Inc

Recalled Item: AirLife Isothermal Breathing Circuit Accessory - Infant Patient Y Connector...

The Issue: The Y adapter within the breathing circuit may spontaneously crack, causing...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 29, 2012· Carefusion 2200 Inc

Recalled Item: AirLife Isothermal Breathing Circuit Recalled by Carefusion 2200 Inc Due to...

The Issue: The Y adapter within the breathing circuit may spontaneously crack, causing...

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

Class I — Serious Health HazardOngoing