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. 2,266 recalls have been distributed to South Dakota in the last 12 months.

47,632 total recalls
2,266 in last 12 months

Showing 4404144060 of 47,632 recalls

Medical DeviceMay 3, 2013· ConMed Corporation

Recalled Item: PadPro(R) Adult Radiotransparent Multifunction Electrodes Recalled by ConMed...

The Issue: ConMed was notified by the contract manufacturer that their wire/connector...

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

Class II — Potential Health HazardOngoing
DrugMay 2, 2013· Hospira Inc.

Recalled Item: Gentamicin Sulfate Injection USP 80 mg/2 mL(40 mg/mL as Gentamicin) Recalled...

The Issue: Presence of Particulate Matter: visible particles were identified floating...

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 2, 2013· Nestle USA, Inc - Northbrook Pizza Head Office

Recalled Item: california Pizza Kitchen crispy thin crust Recalled by Nestle USA, Inc -...

The Issue: Plastic contamination. Four pizzas with specific production codes, are being...

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 2, 2013· Nestle USA, Inc - Northbrook Pizza Head Office

Recalled Item: DiGiorno pizzeria Recalled by Nestle USA, Inc - Northbrook Pizza Head Office...

The Issue: Plastic contamination. Four pizzas with specific production codes, are being...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 2, 2013· Remel Inc

Recalled Item: Streptex* Latex D Recalled by Remel Inc Due to The product may give weak or...

The Issue: The product may give weak or false negative test results.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2013· Remel Inc

Recalled Item: Streptex* kit Recalled by Remel Inc Due to The product may give weak or...

The Issue: The product may give weak or false negative test results.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 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...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2013· Siemens Medical Solutions USA, Inc

Recalled Item: Mobiletta Mira Mobile X-ray System Recalled by Siemens Medical Solutions...

The Issue: Siemens issued a Field Safety Alert about the potential risk to users when...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2013· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Siemens brand MicroScan Dried Negative Breakpoint Combo 47 panels...

The Issue: The product has the potential for false negative or delayed reaction for...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2013· Merit Medical Systems, Inc.

Recalled Item: Merit Medical PerfOrma Anglographic Catheter 5F Multipack Product Usage:...

The Issue: Merit Medical Systems is recalling various lots of Performa Cardiac...

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

Class II — Potential Health HazardOngoing
DrugMay 1, 2013· Beamonstar Products

Recalled Item: Velextra All-Natural Herbal Supplement Recalled by Beamonstar Products Due...

The Issue: Marketed Without an Approved NDA/ANDA; products have been found to contain...

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

Class I — Serious Health HazardOngoing
Refund
DrugMay 1, 2013· Beamonstar Products

Recalled Item: SexVoltz All Natural Herbal Supplement Recalled by Beamonstar Products Due...

The Issue: Marketed Without an Approved NDA/ANDA; products have been found to contain...

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

Class I — Serious Health HazardOngoing
Refund
DrugMay 1, 2013· Medicis Pharmaceutical Corp

Recalled Item: CLENZIderm M.D. Acne Therapeutic System Normal to Oily Skin kit Recalled by...

The Issue: cGMP Deviations; during the production process, CLENZIderm M.D. Daily Foam...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 1, 2013· CooperSurgical, Inc.

Recalled Item: CooperSurgical TransWarmer Infant Transport Mattress with WarmGel P/N 20421...

The Issue: Trans Warmer Infant and Transport Mattress not labeled with exp.date may not...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2013· Elekta, Inc.

Recalled Item: DMLC IV-ERGO Product Usage: Intended for use with rotating gantry Recalled...

The Issue: It is possible for an intermittent error to occur in the gantry sensor of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2013· Becton Dickinson & Company

Recalled Item: BD Vacutainer Multiple Sample and Direct Draw Luer Adapter BD Franklin Lakes...

The Issue: BD Vacutainer Multiple Sample and Direct Draw Luer Adapter may have blood...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2013· Becton Dickinson & Company

Recalled Item: BD SafetyGlide Allergy. Sterile Allergy Treatment Syringe Tray. Recalled by...

The Issue: There has been an increase in complaints regarding the needle/safety...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2013· Applied Medical Resources Corp

Recalled Item: Applied Medicals Epix¿ and Direct Drive Laparoscopic Graspers Recalled by...

The Issue: Applied Medical is conducting a voluntary recall on specific lot numbers of...

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

Class II — Potential Health HazardOngoing
DrugApril 30, 2013· King Legacy, a wholly owned subsidiary of Pfizer

Recalled Item: Levoxyl (levothyroxine sodium) tablets Recalled by King Legacy, a wholly...

The Issue: Subpotent Drug: The products were below specification for potency at the...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 30, 2013· Hi-Tech Pharmacal Co., Inc.

Recalled Item: HydrOXYzine Hydrochloride Oral Solution Recalled by Hi-Tech Pharmacal Co.,...

The Issue: Subpotent; 24 month stability test station

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

Class III — Low RiskOngoing
Refund