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. 2,386 recalls have been distributed to South Dakota in the last 12 months.
Showing 22161–22180 of 27,558 recalls
Recalled Item: Velocity" Biopsy Valve Recalled by US Endoscopy Group Inc Due to The company...
The Issue: The company has received reports of structural non conformance at the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Thumb Screw for the Synthes Recon Locking Aiming Arm for Recalled by...
The Issue: For certain lots, the incorrect raw material of annealed 17-4PH Stainless...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Equinoxe 44mm Short Humeral Head Catalog Number 310-01-44. Orthopedic...
The Issue: Incorrectly packaged. Outer and inner labeling may incorrectly identify the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: - NTL-30 30ml Nutrio Enteral Feeding Syringe (sterile) - NTL-60 Recalled by...
The Issue: The firm is recalling sterile enteral feeding syringes due to determining...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ameda One-Hand Manual Breast Pump (SKU 17161) - Primary packaging Recalled...
The Issue: Devices were not sterilized
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Autostainer Link 48 (AS480) Recalled by Dako North America Inc. Due to A...
The Issue: A false negative result affecting the diagnosis may occur. A defect in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ameda Dual Short Term HygieniKit Milk Collections System (SKU 17115)...
The Issue: Devices were not sterilized
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Triathlon Distal Capture Assembly Catalog No: 6541-1-723 The Triathlon...
The Issue: Potential for weld disassociation of the cross pin, which could lead to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EndoWrist One Vessel Sealer Recalled by Intuitive Surgical, Inc. Due to...
The Issue: Intuitive Surgical has identified the potential for a certain, small portion...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Outer cardboard box labeling: Pinnacle Cure Sleeve Recalled by Sybron Dental...
The Issue: Cases of Cure Sleeve labeled with part number 4513, which fits 13mm tips,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EndoWrist One Vessel Sealer Recalled by Intuitive Surgical, Inc. Due to...
The Issue: Intuitive Surgical has identified the potential for a certain, small portion...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SMARTSET GHV Gentamicin Bone Cement. A self-curing Recalled by DePuy...
The Issue: One lot of SMARTSET GHV Gentamicin Bone Cement is partially agglomerated ....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: G7 Variant Elution Buffer HiS no. 1 (M) component of Recalled by Tosoh...
The Issue: The G7 Variant Elution Buffer HiS no. 1 (M) is incorrectly labeled with an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CooperSurgical PESSARY KIT-CUBE#2 Recalled by CooperSurgical, Inc. Due to...
The Issue: Incorrect size printed on the Milex Pessary Kit packaging label
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Healthcare DuraDiagnost X- Ray Recalled by Philips Medical Systems,...
The Issue: The system is designed to emit a beep upon termination of an exposure....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Healthcare DigitalDiagnost System X-Ray Recalled by Philips Medical...
The Issue: The system is designed to emit a beep upon termination of an exposure....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIEMENS SOMATOM Force with software version VA50A and /or VA50A_FP1 Recalled...
The Issue: Possibility of image artifacts during data acquisition when using Adaptive...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Terumo HX2 Temperature Management System provides temperature control of two...
The Issue: Malfunctioning mixing valve and loss of cooling and/or heating capability....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Computed Tomography X-ray Systems (Brilliance CT 64-channel w/Essence...
The Issue: Philips discovered that a software defect exists in marketed product wherein...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Computed Tomography X-ray Systems Brilliance CT 64-channel with Essence...
The Issue: 5 issues. Fast Get Ready incorrectly enabled during service procedures....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.