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. 2,534 recalls have been distributed to South Dakota in the last 12 months.
Showing 5041–5060 of 27,558 recalls
Recalled Item: SCORPIO U-DOME PATELLA -Intended for knee replacement Part Number: 73-3708...
The Issue: Product manufactured using UHMWPE raw material over 5 years of age has the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SCORPIO U-DOME PATELLA -Intended for knee replacement Part Number: 73-3910...
The Issue: Product manufactured using UHMWPE raw material over 5 years of age has the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Scorpio NRG Tibial Brg Insert Assy -Intended for knee replacement Recalled...
The Issue: Product manufactured using UHMWPE raw material over 5 years of age has the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RGT.LARGE-PCA MOD.REV.- DUR.REV.INSERT Intended for knee replacement Product...
The Issue: Product manufactured using UHMWPE raw material over 5 years of age has the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LEFT LARGE-PCA MOD.REV.DUR.REV.INSERT Intended for knee replacement Part...
The Issue: Product manufactured using UHMWPE raw material over 5 years of age has the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SCORPIO TS TIB INSERT -Intended for knee replacement Part Number: 72-4-0510...
The Issue: Product manufactured using UHMWPE raw material over 5 years of age has the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SERIES II TIBIAL BEAR INSERT-Intended for knee replacement Part Number:...
The Issue: Product manufactured using UHMWPE raw material over 5 years of age has the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SCORPIO TOTAL KNEE MEDIALIZED DOME PATELLA-SZ #5 -Intended for knee Recalled...
The Issue: Product manufactured using UHMWPE raw material over 5 years of age has the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Scorpio NRG Tibial Brg Insert Assy -Intended for knee replacement Recalled...
The Issue: Product manufactured using UHMWPE raw material over 5 years of age has the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SCORPIO TS TIB INSERT. Intended for knee replacement Part Number: 72-4-7518...
The Issue: Product manufactured using UHMWPE raw material over 5 years of age has the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SCORPIO TS TIB INSERT -Intended for knee replacment Part Number: 72-4-7516...
The Issue: Product manufactured using UHMWPE raw material over 5 years of age has the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LARGE PRIMARY REV.TIB.INSERT- DURACON Intended for knee replacement Product...
The Issue: Product manufactured using UHMWPE raw material over 5 years of age has the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOLTIVE SuperPulsed Laser Fibers Model Numbers TFL-FBX150S Recalled by...
The Issue: Olympus identified inconsistencies in the Instructions for Use regarding...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SCORPIO U-DOME PATELLA -Intended for knee replacement Part Number: 73-3508...
The Issue: Product manufactured using UHMWPE raw material over 5 years of age has the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Scorpio-Flex Ttl Kn P-S Tib Brg Insrt Asy- -Intended for Recalled by...
The Issue: Product manufactured using UHMWPE raw material over 5 years of age has the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DURATION A-P LIPPED TIB.INSERT-DURAC Intended for knee replacement Product...
The Issue: Product manufactured using UHMWPE raw material over 5 years of age has the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bkActiv Ultrasound System 2300 Recalled by B-K Medical A/S Due to An issue...
The Issue: An issue on the Dual Live Compare feature on the bkActiv system could result...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Link Patella Glide Resection Guide- For the implantation of the Recalled by...
The Issue: Mislabeled: Angle and height of the device marked as L(large) corresponds to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GammaPod - Treatment Planning System-a component of the GammaPod Irradiation...
The Issue: Wrong structures imported into the GammaPod Treatment Planning...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spectral CT 7500 Recalled by Philips North America Llc Due to Multiple...
The Issue: Multiple software issues that affect device functionality.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.