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. 2,330 recalls have been distributed to South Dakota in the last 12 months.
Showing 34821–34840 of 47,632 recalls
Recalled Item: Shorts on The Beach Golden Edition by Pink Bikini Recalled by Lucy's Weight...
The Issue: Marketed without an approved NDA/ANDA: Product contains undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HARMONIC ACE+ 7 Laparoscopic Shears with Advanced Hemostasis (23cm Recalled...
The Issue: Complaints of holes in Tyvek which can compromise the sterile barrier...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TELETOM EQUIPMENT MANAGEMENT SYSTEM 4 and 6 series TELETOM is Recalled by...
The Issue: During the use of the TELETOM Series 4 & 6 there is potential for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sedalmex (Acetaminophen 500 mg with Caffeine 65 mg) Pain Reliever tablets...
The Issue: Cross Contamination With Other Products: Potential cross-contamination of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Founders Pride Chocolate Chip Cookies 120 - 2.5 oz frozen Recalled by Custom...
The Issue: Product may be contaminated with peanuts.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Goodcents deli fresh subs Fresh Baked Giant Cookie Recalled by Mr Goodcents...
The Issue: Product may be contaminated with peanuts.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Merge Cardio software. Product Usage: Merge Cardio is a system Recalled by...
The Issue: Users can merge a device import file with an image study that already has a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ELITech Clinical Systems reagents used on the Selectra ProS and Recalled by...
The Issue: ELITech Clinical Systems reagents based on Trinder reaction used on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Eon 100 system included the following product numbers and Recalled by...
The Issue: ELITech clinical Systems reagents based on Trinder reaction used on the Eon...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Envoy 500 system includes the following product numbers and Recalled by...
The Issue: ELITech clinical Systems reagents based on Trinder reaction used on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Eon 300 system includes the following product numbers and Recalled by...
The Issue: ELITech clinical Systems reagents based on Trinder reaction used on the Eon...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sentinel MULTIGENT Ammonia Ultra Reagent Recalled by Sentinel CH SpA Due to...
The Issue: Results for ammonia are below the linear range of the assay for samples that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baby Omega 3 Dietary supplement (in liquid form) Recalled by Zarbee's...
The Issue: Some units of each lot may contain contaminants (elevated aerobic plate...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Baby Vitamin D Dietary supplement (in liquid form) Recalled by Zarbee's...
The Issue: Some units of each lot may contain contaminants (elevated aerobic plate...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Valeant Pharmaceuticals North America Recalled by Valeant Pharmacueticals...
The Issue: The Serial I.D. Label and some information in the Operation Manual for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOMET 3i Recalled by Biomet 3i, LLC Due to Inadequate biocompatibility testing.
The Issue: Inadequate biocompatibility testing.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOMET 3i Recalled by Biomet 3i, LLC Due to Inadequate biocompatibility testing.
The Issue: Inadequate biocompatibility testing.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOMET 3i Recalled by Biomet 3i, LLC Due to Inadequate biocompatibility testing.
The Issue: Inadequate biocompatibility testing.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOMET 3i Recalled by Biomet 3i, LLC Due to Inadequate biocompatibility testing.
The Issue: Inadequate biocompatibility testing.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Orthopaedics Duracon Flat Tibial Wedge Cemented use only Sterile....
The Issue: Stryker Orthopaedics has received two customer complaints regarding Duracon...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.