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. 2,349 recalls have been distributed to South Dakota in the last 12 months.

47,632 total recalls
2,349 in last 12 months

Showing 2612126140 of 47,632 recalls

DrugDecember 14, 2017· Boehringer Ingelheim Pharmaceuticals, Inc.

Recalled Item: SPIRIVA HandiHaler (tiotropium bromide inhalation powder) 18 mcg/capsule (90...

The Issue: Failed Stability Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 14, 2017· SHISEIDO AMERICA INC.

Recalled Item: Shiseido Future Solution LX Universal Defense SPF 50+ (octinoxate 4.9%...

The Issue: GMP Deviations: manufacturing of API material did not meet GMP and quality...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 14, 2017· SHISEIDO AMERICA INC.

Recalled Item: Shiseido Future Solution LX Discovery Set contains SPF 50+ (octinoxate 4.9%...

The Issue: GMP Deviations: manufacturing of API material did not meet GMP and quality...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 14, 2017· SHISEIDO AMERICA INC.

Recalled Item: bareMinerals Broad Spectrum SPF 50 Daily Prep Lotion (zinc oxide 23.8%...

The Issue: GMP Deviations: manufacturing of API material did not meet GMP and quality...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 14, 2017· Teva Pharmaceuticals USA

Recalled Item: Moexipril Hydrochloride and Hydrocholorothiazide Tablets USP Recalled by...

The Issue: Failed Impurities/Degradation Specifications: High out of specification test...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 14, 2017· SHISEIDO AMERICA INC.

Recalled Item: Shiseido Future Solutions LX Triple Points Bonus contains SPF 50+ Recalled...

The Issue: GMP Deviations: manufacturing of API material did not meet GMP and quality...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 14, 2017· Abbott Gmbh & Co. KG

Recalled Item: ARCHITECT DHEA-S Reagent Product Usage: It is a chemiluminescent...

The Issue: Falsely elevated results may be obtained when using the ARCHITECT DHEA-S...

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

Class II — Potential Health HazardOngoing
DrugDecember 13, 2017· ALLERGAN

Recalled Item: INFeD (Iron Dextran Injection USP) 100 mg elemental iron/2 ml (50 mg/mL)...

The Issue: Failed Stability Specifications: Product stability testing results did not...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 13, 2017· Halyard Health, Inc

Recalled Item: CORTRAK* 2 Nasogastric/Nasointestinal (NG/NI) Feeding Tubes with...

The Issue: The transmitting stylet within CORTRAK* 2 nasogastric/Nasointestinal (NG/NI)...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 13, 2017· Covidien LLC

Recalled Item: Signia" Power Handle (SIGPHANDLE Recalled by Covidien LLC Due to Product...

The Issue: Product reportedly shutting down during use.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2017· Boston Scientific Corporation

Recalled Item: Malecot Nephrostomy Catheter Set Recalled by Boston Scientific Corporation...

The Issue: Certain Malecot Nephrostomy Catheters are breaking at the mid-shaft bond...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2017· Boston Scientific Corporation

Recalled Item: Malecot Nephrostomy Catheter Set Recalled by Boston Scientific Corporation...

The Issue: Certain Malecot Nephrostomy Catheters are breaking at the mid-shaft bond...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2017· Boston Scientific Corporation

Recalled Item: Percutaneous Access Set Recalled by Boston Scientific Corporation Due to...

The Issue: Certain Malecot Nephrostomy Catheters are breaking at the mid-shaft bond...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2017· Boston Scientific Corporation

Recalled Item: Re-Entry" Malecot Nephrostomy Catheter Set Recalled by Boston Scientific...

The Issue: Certain Malecot Nephrostomy Catheters are breaking at the mid-shaft bond...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2017· Boston Scientific Corporation

Recalled Item: Re-Entry" Malecot Nephrostomy Catheter Set Recalled by Boston Scientific...

The Issue: Certain Malecot Nephrostomy Catheters are breaking at the mid-shaft bond...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2017· Boston Scientific Corporation

Recalled Item: Malecot Nephrostomy Catheter System Recalled by Boston Scientific...

The Issue: Certain Malecot Nephrostomy Catheters are breaking at the mid-shaft bond...

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

Class II — Potential Health HazardOngoing
DrugDecember 12, 2017· Keryx Biopharmaceuticals, Inc.

Recalled Item: Auryxia (ferric citrate) tablets Recalled by Keryx Biopharmaceuticals, Inc....

The Issue: Presence of Foreign Substance: Reports have been received of damaged...

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

Class III — Low RiskOngoing
Refund
FoodDecember 12, 2017· Rachael's Food Corporation

Recalled Item: SPRINGFIELD SMOKED Whitefish Meat Recalled by Rachael's Food Corporation Due...

The Issue: Product may be contaminated with Listeria monocytogenes.

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

Class I — Serious Health HazardOngoing
Refund
FoodDecember 12, 2017· Rachael's Food Corporation

Recalled Item: SPRINGFIELD SMOKED FISH Smoked Sable Recalled by Rachael's Food Corporation...

The Issue: Product may be contaminated with Listeria monocytogenes.

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

Class I — Serious Health HazardOngoing
Refund
FoodDecember 12, 2017· Rachael's Food Corporation

Recalled Item: RACHAEL'S SPRINGFIELD SMOKED FISH PASTRAMI LOX Recalled by Rachael's Food...

The Issue: Product may be contaminated with Listeria monocytogenes.

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

Class I — Serious Health HazardOngoing
Refund