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. 1,059 recalls have been distributed to Kansas in the last 12 months.

50,117 total recalls
1,059 in last 12 months

Showing 14141–14160 of 28,538 recalls

Medical DeviceApril 9, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: Artis Zeego (material 10280959) - Product Usage: AXIOM Artis zee Recalled by...

The Issue: In affected Artis systems the movement of the floating tabletop may be...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 9, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: Artis Q (material 10848280 Recalled by Siemens Medical Solutions USA, Inc...

The Issue: In affected Artis systems the movement of the floating tabletop may be...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 9, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: Artis Zee (material # 10094135 Recalled by Siemens Medical Solutions USA,...

The Issue: In affected Artis systems the movement of the floating tabletop may be...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 9, 2019· Microbiologics Inc

Recalled Item: Cepheid Xpert SA Nasal Complete Control Panel (Catalog #8196) UDI: Recalled...

The Issue: Product with incorrect shelf life.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 9, 2019· Microbiologics Inc

Recalled Item: Cepheid Xpert MRSA/MRSA NxG Control Panel (Catalog #8195) UDI:...

The Issue: Product with incorrect shelf life.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 9, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: Artis Q (material 10848280 Recalled by Siemens Medical Solutions USA, Inc...

The Issue: In affected Artis systems the movement of the floating tabletop may be...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2019· Zimmer GmbH

Recalled Item: CBS 4.0 countersink Recalled by Zimmer GmbH Due to An investigation...

The Issue: An investigation identified that the products were possibly manufactured...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2019· Zimmer GmbH

Recalled Item: Drill Recalled by Zimmer GmbH Due to An investigation identified that the...

The Issue: An investigation identified that the products were possibly manufactured...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2019· Zimmer GmbH

Recalled Item: Drill for 2.7mm screw Recalled by Zimmer GmbH Due to An investigation...

The Issue: An investigation identified that the products were possibly manufactured...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2019· Zimmer GmbH

Recalled Item: Drill Recalled by Zimmer GmbH Due to An investigation identified that the...

The Issue: An investigation identified that the products were possibly manufactured...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2019· Zimmer GmbH

Recalled Item: CBS 7.5 tap Recalled by Zimmer GmbH Due to An investigation identified that...

The Issue: An investigation identified that the products were possibly manufactured...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2019· Zimmer GmbH

Recalled Item: Drill for 2.7mm screw Recalled by Zimmer GmbH Due to An investigation...

The Issue: An investigation identified that the products were possibly manufactured...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2019· Zimmer GmbH

Recalled Item: V-TEK" Recalled by Zimmer GmbH Due to An investigation identified that the...

The Issue: An investigation identified that the products were possibly manufactured...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2019· Compass Health Brands (Corporate Office)

Recalled Item: MediPress pneumatic compression system Recalled by Compass Health Brands...

The Issue: Product design change did not receive proper premarket clearance and lacks a...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2019· Zimmer GmbH

Recalled Item: Drill Recalled by Zimmer GmbH Due to An investigation identified that the...

The Issue: An investigation identified that the products were possibly manufactured...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2019· Zimmer GmbH

Recalled Item: Drill Recalled by Zimmer GmbH Due to An investigation identified that the...

The Issue: An investigation identified that the products were possibly manufactured...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2019· Zimmer GmbH

Recalled Item: Drill Recalled by Zimmer GmbH Due to An investigation identified that the...

The Issue: An investigation identified that the products were possibly manufactured...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2019· Zimmer GmbH

Recalled Item: Drill Recalled by Zimmer GmbH Due to An investigation identified that the...

The Issue: An investigation identified that the products were possibly manufactured...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2019· Zimmer GmbH

Recalled Item: Drill for 2.7mm screw Recalled by Zimmer GmbH Due to An investigation...

The Issue: An investigation identified that the products were possibly manufactured...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2019· Zimmer GmbH

Recalled Item: Drill for 2.7mm screw Recalled by Zimmer GmbH Due to An investigation...

The Issue: An investigation identified that the products were possibly manufactured...

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

Class II — Potential Health HazardOngoing