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. 2,620 recalls have been distributed to Kansas in the last 12 months.

50,117 total recalls
2,620 in last 12 months

Showing 36813700 of 28,538 recalls

Medical DeviceJune 14, 2024· Medical Depot Inc.

Recalled Item: Nitro Glide Knee Walker-offers users recovering from a below-the-knee injury...

The Issue: The tiller separates from the base/front caster assembly. If the knee walker...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2024· Medical Depot Inc.

Recalled Item: Nitro Glide Knee Walker-offers users recovering from a below-the-knee injury...

The Issue: The tiller separates from the base/front caster assembly. If the knee walker...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 13, 2024· Steris Corporation

Recalled Item: Hookup Model/Catalog Number: 2-8-540CAS Product Description: Hookups provide...

The Issue: IFU for hookup were incorrectly within hookup IFUs and online system, Hookup...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 13, 2024· Steris Corporation

Recalled Item: Hookup Model/Catalog Number: 2-8-540 Product Description: Hookups provide...

The Issue: IFU for hookup were incorrectly within hookup IFUs and online system, Hookup...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 13, 2024· Steris Corporation

Recalled Item: Hookup Model/Catalog Number: 2-8-540HAN Product Description: Hookups provide...

The Issue: IFU for hookup were incorrectly within hookup IFUs and online system, Hookup...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 13, 2024· Steris Corporation

Recalled Item: Hookup Model/Catalog Number: DSD-110-HU0163 Product Description: Hookups...

The Issue: IFU for hookup were incorrectly within hookup IFUs and online system, Hookup...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 13, 2024· Hologic Inc

Recalled Item: Horizon X-Ray Bone Densitometer (DXA) Models: Horizon-A Recalled by Hologic...

The Issue: Non-conformance pertains to electromagnetic compatibility requirements...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2024· Boston Scientific Corporation

Recalled Item: Autotome RX 20mm CUT WIRE Cannulating Sphincterotome Recalled by Boston...

The Issue: Foreign material may be present on the enclosed section of the cutting wire...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2024· Synergetics Inc

Recalled Item: BAUSCH+LOMB Recalled by Synergetics Inc Due to Sterilization certificates...

The Issue: Sterilization certificates could not be validated by the supplier

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 12, 2024· Synergetics Inc

Recalled Item: BAUSCH+LOMB Recalled by Synergetics Inc Due to Sterilization certificates...

The Issue: Sterilization certificates could not be validated by the supplier

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 12, 2024· Synergetics Inc

Recalled Item: BAUSCH+LOMB Recalled by Synergetics Inc Due to Sterilization certificates...

The Issue: Sterilization certificates could not be validated by the supplier

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 12, 2024· Synergetics Inc

Recalled Item: BAUSCH+LOMB Recalled by Synergetics Inc Due to Sterilization certificates...

The Issue: Sterilization certificates could not be validated by the supplier

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 11, 2024· Medical Action Industries, Inc. 306

Recalled Item: Foam Protective Pouches Recalled by Medical Action Industries, Inc. 306 Due...

The Issue: The protective pouches were identified to have been improperly labeled with...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2024· Merit Medical Systems, Inc.

Recalled Item: Various Merit Medical convenience kits that contain recalled Jiangsu Shenli...

The Issue: Medical convenience kits contain plastic syringes affected by the FDA Safety...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2024· Merit Medical Systems, Inc.

Recalled Item: Various Merit Medical convenience kits that contain recalled Jiangsu Shenli...

The Issue: Medical convenience kits contain plastic syringes affected by the FDA Safety...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2024· Merit Medical Systems, Inc.

Recalled Item: Various Merit Medical convenience kits that contain recalled Jiangsu Shenli...

The Issue: Medical convenience kits contain plastic syringes affected by the FDA Safety...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2024· Merit Medical Systems, Inc.

Recalled Item: Various Merit Medical convenience kits that contain recalled Jiangsu Shenli...

The Issue: Medical convenience kits contain plastic syringes affected by the FDA Safety...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2024· Merit Medical Systems, Inc.

Recalled Item: Various Merit Medical convenience kits that contain recalled Jiangsu Shenli...

The Issue: Medical convenience kits contain plastic syringes affected by the FDA Safety...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2024· Merit Medical Systems, Inc.

Recalled Item: Various Merit Medical convenience kits that contain recalled Jiangsu Shenli...

The Issue: Medical convenience kits contain plastic syringes affected by the FDA Safety...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2024· Merit Medical Systems, Inc.

Recalled Item: Various Merit Medical convenience kits that contain recalled Jiangsu Shenli...

The Issue: Medical convenience kits contain plastic syringes affected by the FDA Safety...

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

Class II — Potential Health HazardOngoing