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. 1,060 recalls have been distributed to South Dakota in the last 12 months.
Showing 8141–8160 of 27,558 recalls
Recalled Item: 11278VSA 11278VSAK Flexible Video-Uretero-Renoscope (FLEX-XC) Z23117US-BA...
The Issue: Failure to achieve the expected six-log reduction in microorganisms...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 11001RD1 11001RDK1 KARL STORZ Slim Nasopharyngolaryngoscope 96216006US V5.0...
The Issue: Failure to achieve the expected six-log reduction in microorganisms...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 11278VSA 11278VSAK Flexible Video-Uretero-Renoscope (FLEX-XC) Z23117US-BA...
The Issue: Failure to achieve the expected six-log reduction in microorganisms...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 11272V CMOS VIDEO-CYSTO-URETHROSCOPE REV 11272VA 11272VAK CMOS...
The Issue: Failure to achieve the expected six-log reduction in microorganisms...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 11005BC1 11005BCK1 Flexible Bronchoscope Z21493US-BA (06/2019) Recalled by...
The Issue: Failure to achieve the expected six-log reduction in microorganisms...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 11272VN 11272VNK Flexible Video Urethro Cystoscope Z18442US-BD (08/2018)...
The Issue: Failure to achieve the expected six-log reduction in microorganisms...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 11278A2 11278AK2 Flexible Ureteroscope Z20615US-BA (08-2018) Recalled by...
The Issue: Failure to achieve the expected six-log reduction in microorganisms...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 11272VUE 11272VUEK Flexible Video Cysto-Urethroscope 96136031USCA V1.1...
The Issue: Failure to achieve the expected six-log reduction in microorganisms...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CooperSurgical H/S CATHETER SET FR 5 with Integated Stylet Model: Recalled...
The Issue: Incorrect bonding material used for assembly of the catheter, may fail,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cooper Surgical H/S ELLIPTOSPHERE CATH 5 Fr -For administering contrast...
The Issue: Incorrect bonding material used for assembly of the catheter, may fail,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus DISPOSABLE GRASPING FORCEPS Recalled by Olympus Corporation of the...
The Issue: Forceps do not comply with Olympus standards for the amount of force...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cooper Surgical H/S ELLIPTOSPHERE CATH 5 FR Set-For administering contrast...
The Issue: Incorrect bonding material used for assembly of the catheter, may fail,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Instructions for Use Recalled by Medtronic Inc Due to Errors and...
The Issue: Errors and inconsistencies that were identified in the Instruction for Use...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The VerifyNow P2Y12 Test is designed to measure platelet P2Y12 Recalled by...
The Issue: Two whole blood Platelet Reactivity tests exist that share the same reagent...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Percept BrainSense Implantable Neurostimulator (INS) Recalled by Medtronic...
The Issue: The Implantable Neurostimulator (INS) cannot communicate with the clinical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HydroMARK Breast Biopsy Marker Recalled by Devicor Medical Products Inc Due...
The Issue: Small patient labels do not match the primary device label. The primary...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Invacare TDX SP2 Recalled by Invacare Corporation Due to The battery wiring...
The Issue: The battery wiring harness on affected wheelchairs may become disconnected...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Percept PC BrainSense Implantable Neurostimulator (INS) Model B35200...
The Issue: The Implantable Neurostimulator (INS) cannot communicate with the clinical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Triathlon Tritanium Tibial Component (Size 6) Recalled by Howmedica...
The Issue: Stryker has discovered a potential product mix where the size of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vanta INS Implantable Neurostimulator. Medtronic Model 977006 Vanta with...
The Issue: The Implantable Neurostimulator Model may be susceptible to not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.