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 21381–21400 of 27,558 recalls
Recalled Item: ASP-1021 LipoTower with Aspiration Pump and Tumescent Pump. Medical use....
The Issue: There is potential risk of electrical shock if lead wires inside the device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ATTUNE CONV RP CR ARTICULATION SURFACE SZ1 Recalled by DePuy Orthopaedics,...
The Issue: Potential for the Balseal, a small wire spring coil located on the post...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: On-X Prosthetic Heart Valve Product Usage: Indicated for the replacement...
The Issue: Incorrect product label. The type of Sewing Ring was mislabeled as being a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: JustRight 5mm Stapler Recalled by Justright Surgical, LLC Due to JustRight...
The Issue: JustRight Surgical is recalling various lots of JustRight 5mm Stapler...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: JustRight 5mm Reload Recalled by Justright Surgical, LLC Due to JustRight...
The Issue: JustRight Surgical is recalling various lots of JustRight 5mm Stapler...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARCHITECT c8000 System List Number 01G06-98 Product Usage: The Abbott...
The Issue: The ARCHITECT c8000 instrument contains tubing that does not meet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Magnus Hybrid OR Table Column (1180.01B2) used in conjunction with Recalled...
The Issue: There is a potential issue that could result to collision between the C-arm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Helical Blade Inserter for Trochanteric Fixation Nail-ADVANCED (TFNA)...
The Issue: The height of one of the three guiding pins of the Helical Blade Inserter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NDI Disposable Marker Spheres for Brainlab IGS (Image Guided Recalled by...
The Issue: Inadequate curing of adhesive, may cause the two halves of the spheres to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Offset Femoral Alignment Guide Recalled by Omnilife Science Inc. Due to The...
The Issue: The markings on both versions of the OFFSET FEMORAL ALIGNMENT GUIDES are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nakoma-SL Anterior Cervical Plating System's Variable Single Barrel Drill...
The Issue: Inadequate interference between the screw and the plate when screw implanted...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Scientific Solutions Americas Analytical X-ray System. Delta...
The Issue: Higher than published scatter around the probe head when testing some...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Offset Femoral Alignment Guide 4mm x 6¿ Recalled by Omnilife Science Inc....
The Issue: The markings on both versions of the OFFSET FEMORAL ALIGNMENT GUIDES are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips HeartStart XL+ Defibrillator/Monitor Product Usage: The HeartStart...
The Issue: Multiple software and hardware issues with device that can affect its function.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cochlear Nucleus Sterile Silicone Template Product Usage: The Cochlear ...
The Issue: Cochlear Americas is recalling Nucleus Sterile Silicone Template...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: APEX INTERFACE Hemi 54X and Flared 56X Recalled by Omnilife Science Inc. Due...
The Issue: The device may have improper screw hole placement due to inaccurate location...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Volcano PV .035 Catheter: Part number: 88901 Recalled by Volcano Corporation...
The Issue: During a relabeling procedure at the manufacturing facility, the products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prestige Plus 185cm J-Tip: Part number: 9185J Recalled by Volcano...
The Issue: During a relabeling procedure at the manufacturing facility, the products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Emotion 16 Recalled by Siemens Medical Solutions USA, Inc Due to A...
The Issue: A potential safety issue involving two (2) broken screws and one (1) bowed,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Emotion 6 Recalled by Siemens Medical Solutions USA, Inc Due to A...
The Issue: A potential safety issue involving two (2) broken screws and one (1) bowed,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.