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. 2,260 recalls have been distributed to South Dakota in the last 12 months.
Showing 45241–45260 of 47,632 recalls
Recalled Item: SOL SYS F 9 CALC L 13.5MM LG Packaging: Product Recalled by DePuy...
The Issue: An Engineering Analysis has determined the Solution Calcar Stem has the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOL SYS L 9IN CALC 2.25/16.5 Packaging: Product is packed Recalled by DePuy...
The Issue: An Engineering Analysis has determined the Solution Calcar Stem has the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOL SYS 8IN CALCAR SZ12 Packaging: Product is packed within a poly protector...
The Issue: An Engineering Analysis has determined the Solution Calcar Stem has the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Carisoprodol Tablets Recalled by West-ward Pharmaceutical Corp. Due to...
The Issue: Labeling: Not elsewhere classified: On 12/12/11, DEA published a final rule...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lisinopril and Hydrochlorothiazide Tablets Recalled by West-ward...
The Issue: Presence of Foreign Substance: Reports of gray smudges identified as minute...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Pure Apricot Pecan Flats Recalled by Unified Grocers Inc. Due to Undeclared...
The Issue: Unified Grocers is recalling Pure Apricot Pecan Flats because it may contain...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Set Screw 5.5 mm Rod - Model #7703-1600. Product Usage: Recalled by Biomet...
The Issue: Biomet Spine LLC is recalling the Set Screw 5.5 mm Rod due to the set screw...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Eon and Eon Mini charging system Recalled by St. Jude Medical Due to There...
The Issue: There is issues of warmth or heating at the implant site during charging for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Handset component of the Handicare USA's Minivator Bath Bliss Reclining...
The Issue: Firm became aware that two handsets in the affected batches became...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CO2 Incubators (General Purpose Incubator) Recalled by Thermo Fisher...
The Issue: Incubators manufactured prior to mid 2009 have coated metal hinges that have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mobile Diagnostic X-Ray System with Digital Panel Recalled by Philips...
The Issue: When the operator moves an image to another view then the electronic marker...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Beckman Coulter AU5800 Clinical Chemistry Analyzer. An automated chemistry...
The Issue: Due to a software data storage limitation which only occurs under certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mindray DS USA Recalled by Mindray DS USA, Inc. d.b.a. Mindray North America...
The Issue: Mindray has identified a software anomaly that may where, in the presence of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pinnacle Cancellous Screw Packaging: Product is housed within a polyurethane...
The Issue: DePuy Orthopaedics, Inc. is issuing a voluntary recall of ten lots of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TCM4 series Base Units Recalled by Radiometer America Inc Due to RADIOMETER...
The Issue: RADIOMETER became aware that the TCM4 series Base Unit does not comply with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Somatom CTs equipped with software syngo CT2010A Recalled by Siemens...
The Issue: Sporadic hang-up malfunctions concerning 3D reconstructions during activated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TORISEL Kit (temsirolimus) injection Recalled by Pfizer Inc. Due to Lack of...
The Issue: Lack of Assurance of Sterility; potential that a low level of endotoxins may...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fresenius GranuFlo Dry Acid Concentrate For Bicarbonate Dialysis 2.0 K...
The Issue: GranuFlo Dry Acid Concentrate may show discoloration
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Axiom Artis zeego systems with software version VC14 Recalled by...
The Issue: In the course of the firm's product monitoring activities, a potential risk...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custom Breast Biopsy Tray w/Sodium Chloride Recalled by Custom Healthcare...
The Issue: Surgical procedure trays are packed with pharmaceuticals for injection that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.