Product Recalls in Kansas

Product recalls affecting Kansas — including food, drugs, consumer products, medical devices, and vehicles distributed to Kansas. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,565 recalls have been distributed to Kansas in the last 12 months.

50,117 total recalls
2,565 in last 12 months

Showing 1318113200 of 28,538 recalls

Medical DeviceAugust 15, 2019· Zimmer Biomet, Inc.

Recalled Item: Vanguard XP Tibial Tray 83 mm Item # 195253 Recalled by Zimmer Biomet, Inc....

The Issue: The locking bar not fully engaging

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2019· Zimmer Biomet, Inc.

Recalled Item: XP-XP Tibial Tray - Interlok 91mm Item # 195761 Recalled by Zimmer Biomet,...

The Issue: The locking bar not fully engaging

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 14, 2019· Bard Peripheral Vascular Inc

Recalled Item: Bard Conquest 40 PTA Dilation Catheter Recalled by Bard Peripheral Vascular...

The Issue: The catheter packaging incorrectly listed the balloon size as 8mm X 20mm...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 14, 2019· WOM World of Medicine AG

Recalled Item: Aquilex Fluid Control System component: Bag deflector Recalled by WOM World...

The Issue: The deficit displayed by the pump can differ from the real deficit, leading...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 14, 2019· Siemens Healthcare Diagnostics, Inc

Recalled Item: Atellica IM anti-CCP IgG (aCCP) Assay Siemens Material Number: 10732998...

The Issue: Atellica IM anti-CCP IgG (aCCP) Test Definition (TDef) Mitigation...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2019· LivaNova USA Inc

Recalled Item: VNS Therapy SENTIVA Generator Model # 1000 Labeling 26-0009-6800 Model...

The Issue: Firm identified a subset of its generators that were sterilized one...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2019· Ethicon, Inc.

Recalled Item: STRATAFIX Spiral PDS Plus Violet 27 (70cm) CTX Needle Product Recalled by...

The Issue: The product does not meet certain internal strength testing specifications.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2019· Roche Diagnostics Operations, Inc.

Recalled Item: AssayTip/AssayCup Tray-used on the cobas e 801 module which is Recalled by...

The Issue: AssayTips part of the AssayTip/AssayCup Tray Tips used on the cobas e 801...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2019· Ethicon, Inc.

Recalled Item: STRATAFIX Spiral PDS Plus Violet 18 (45cm) CT-1 Needle Product Recalled by...

The Issue: The product does not meet certain internal strength testing specifications.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2019· Baxter Healthcare Corporation

Recalled Item: EXACTAMED Oral Dispensers Recalled by Baxter Healthcare Corporation Due to...

The Issue: Exactamed 5 mL Oral Dispenser Pharmacy Packs may contain both 5 mL and 3 mL...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing
Medical DeviceAugust 12, 2019· Zeus Scientific, Inc.

Recalled Item: ZEUS ELISA Parvovirus B19 IgM Test System Recalled by Zeus Scientific, Inc....

The Issue: FDA inspection identified that due to increased positivity (false positives)...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 12, 2019· Varian Medical Systems, Inc.

Recalled Item: Varian Multileaf Collimator [MLC] Recalled by Varian Medical Systems, Inc....

The Issue: After a recent upgrade to the collimator software version 8.5, the firm...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2019· Medtronic Navigation, Inc.

Recalled Item: Medtronic Nexframe Stereotactic System and StealthStation Cranial software...

The Issue: Entry point and lead placement inaccuracies during deep brain stimulation...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceAugust 9, 2019· Nobel Biocare Usa Llc

Recalled Item: Esthetic Abutment CC RP 1.5 mm pre-manufactured prosthetic components...

The Issue: Packages of abutments may contain an incorrect screw. While the screw will...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2019· Nobel Biocare Usa Llc

Recalled Item: Temporary Abutment Engaging CC RP pre-manufactured prosthetic components...

The Issue: Packages of abutments may contain an incorrect screw. While the screw will...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2019· Nobel Biocare Usa Llc

Recalled Item: Universal Base CC RP 1.5 mm Recalled by Nobel Biocare Usa Llc Due to...

The Issue: Packages of abutments (universal base) may contain an incorrect screw. While...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2019· Nobel Biocare Usa Llc

Recalled Item: Temporary Snap Abutment Engaging CC RP 1.5 mm Recalled by Nobel Biocare Usa...

The Issue: Packages of abutments may contain an incorrect screw. While the screw will...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2019· Nobel Biocare Usa Llc

Recalled Item: Temporary Abutment Non-Engaging CC RP pre-manufactured prosthetic components...

The Issue: Packages of abutments may contain an incorrect screw. While the screw will...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2019· Nobel Biocare Usa Llc

Recalled Item: Snappy Abutment 5.5 CC RP 3 mm Recalled by Nobel Biocare Usa Llc Due to...

The Issue: Packages of abutments may contain an incorrect screw. While the screw will...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2019· Randox Laboratories Ltd.

Recalled Item: Liquid Protein Calibrators (SP CAL (LIQ)) Catalogue Number: IT2691 GTIN:...

The Issue: The assigned value for Rheumatoid Factor over recovers against the material...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing