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. 1,660 recalls have been distributed to South Dakota in the last 12 months.
Showing 44981–45000 of 47,632 recalls
Recalled Item: BARD Biopsy Systems (A Business Unit of Bard Peripheral Vascular Recalled by...
The Issue: Bard Peripheral Vascular (BPV) is initiating this recall because a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Plastic bottle containing 10.5 mL of IgM Conjugate Product Usage: Recalled...
The Issue: Affected products have a labeled expiration date of one year too long.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BARD Biopsy Systems (A Business Unit of Bard Peripheral Vascular Recalled by...
The Issue: Bard Peripheral Vascular (BPV) is initiating this recall because a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medi-bolic Booster Injectable (methionine 8.3 mg/mL Recalled by RX South LLC...
The Issue: CGMP Deviations: Pharmaceutical for injection was not manufactured according...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: IRINOTECAN HYDROCHLORIDE INJECTION Recalled by Fresenius Kabi USA LLC (FK...
The Issue: Crystallization: Active pharmaceutical ingredient is precipitating in...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Syeda (drospirenone and ethinyl estradiol) Recalled by Sandoz Incorporated...
The Issue: Tablet/Capsule Imprinted with Wrong ID; a portion of the tablets could...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cardinal Health hCG Cassette Rapid Test Recalled by Alere San Diego, Inc....
The Issue: Alere San Diego Inc. is recalling the Cardinal Health hCG Cassette Rapid...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Advantx Recalled by GE Healthcare, LLC Due to A locking nut...
The Issue: A locking nut might loosen out of the overhead Video Monitor Suspension yoke...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lifeguard Infusion Set with Smartsite Recalled by Churchill Medical Systems,...
The Issue: The label on the device states that the item number is CLGY-2210 when the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pamela's Peanut Butter Chocolate Chip Cookies Recalled by Pamela's Products,...
The Issue: Firm received complaints for on four (4) products which may contain glass or...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Pamela's Baking and Pancake Mix Recalled by Pamela's Products, Inc. Due to...
The Issue: Firm received complaints for on four (4) products which may contain glass or...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Pamela's Chocolate Chunk Cookie Mix Recalled by Pamela's Products, Inc. Due...
The Issue: Firm received complaints for on four (4) products which may contain glass or...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Pamela's Chocolate Cake Mix Recalled by Pamela's Products, Inc. Due to Firm...
The Issue: Firm received complaints for on four (4) products which may contain glass or...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Aesculap Bipolar Generator Foot Pedal Recalled by Aesculap, Inc. Due to The...
The Issue: The bipolar energy did not stop after release of the foot pedal.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Elekta Recalled by Elekta, Inc. Due to If the Apex collimator is incorrectly...
The Issue: If the Apex collimator is incorrectly installed on the radiation head, a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Chenica Gunnell Rehab Series of Wheelchairs (GRSW) Recalled by CHENICA INC....
The Issue: The wheelchairs may not meet the specifications of WC-19 (crash testing),...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: St. Jude Medical Recalled by St Jude Medical Inc Due to The distal end of...
The Issue: The distal end of the core wire of the TorqVue FX Delivery System could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Select Brand Cough Control CF Max Recalled by Aaron Industries Inc Due to...
The Issue: Presence of Precipitate; white substance confirmed as Guaifenesin, an active...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Wal-Mart Equate Tussin CF Adult Maximum Strength Recalled by Aaron...
The Issue: Presence of Precipitate; white substance confirmed as Guaifenesin, an active...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Rite Aid Maximum Strength Tussin Cough & Cold Mucus Relief CF Recalled by...
The Issue: Presence of Precipitate; white substance confirmed as Guaifenesin, an active...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.