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. 2,610 recalls have been distributed to Kansas in the last 12 months.

50,117 total recalls
2,610 in last 12 months

Showing 62016220 of 50,117 recalls

Medical DeviceMarch 20, 2024· Zimmer, Inc.

Recalled Item: ZPLP (Zimmer Periarticular Locking Plate System) Distal Lateral Fibular...

The Issue: Thread form issue for the locking holes in that the locking screws may not...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2024· Zimmer, Inc.

Recalled Item: ZPLP (Zimmer Periarticular Locking Plate System) Distal Lateral Fibular...

The Issue: Thread form issue for the locking holes in that the locking screws may not...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2024· Zimmer, Inc.

Recalled Item: ZPLP (Zimmer Periarticular Locking Plate System) Distal Lateral Fibular...

The Issue: Thread form issue for the locking holes in that the locking screws may not...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2024· Zimmer, Inc.

Recalled Item: ZPLP Distal Lateral Fibular Plate Recalled by Zimmer, Inc. Due to Thread...

The Issue: Thread form issue for the locking holes in that the locking screws may not...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2024· Zimmer, Inc.

Recalled Item: ZPLP (Zimmer Periarticular Locking Plate System) Distal Lateral Fibular...

The Issue: Thread form issue for the locking holes in that the locking screws may not...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2024· Zimmer, Inc.

Recalled Item: ZPLP (Zimmer Periarticular Locking Plate System) Distal Lateral Fibular...

The Issue: Thread form issue for the locking holes in that the locking screws may not...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2024· Zimmer, Inc.

Recalled Item: ZPLP(Zimmer Periarticular Locking Plate System) Distal Lateral Fibular Plate...

The Issue: Thread form issue for the locking holes in that the locking screws may not...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2024· Zimmer, Inc.

Recalled Item: ZPLP Distal Lateral Fibular Plate Recalled by Zimmer, Inc. Due to Thread...

The Issue: Thread form issue for the locking holes in that the locking screws may not...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2024· Zimmer, Inc.

Recalled Item: ZPLP Distal Lateral Fibular Plate Recalled by Zimmer, Inc. Due to Thread...

The Issue: Thread form issue for the locking holes in that the locking screws may not...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2024· Zimmer, Inc.

Recalled Item: ZPLP Distal Lateral Fibular Plate Recalled by Zimmer, Inc. Due to Thread...

The Issue: Thread form issue for the locking holes in that the locking screws may not...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2024· Zimmer, Inc.

Recalled Item: ZPLP Distal Lateral Fibular Plate Recalled by Zimmer, Inc. Due to Thread...

The Issue: Thread form issue for the locking holes in that the locking screws may not...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2024· Zimmer, Inc.

Recalled Item: ZPLP (Zimmer Periarticular Locking Plate System) Distal Lateral Fibular...

The Issue: Thread form issue for the locking holes in that the locking screws may not...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2024· Zimmer, Inc.

Recalled Item: ZPLP (Zimmer Periarticular Locking Plate System) Distal Lateral Fibular...

The Issue: Thread form issue for the locking holes in that the locking screws may not...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2024· Zimmer, Inc.

Recalled Item: ZPLP (Zimmer Periarticular Locking Plate System) Distal Lateral Fibular...

The Issue: Thread form issue for the locking holes in that the locking screws may not...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2024· Abbott Molecular, Inc.

Recalled Item: Alinity m System Recalled by Abbott Molecular, Inc. Due to The Alinity m...

The Issue: The Alinity m System camera detects whether tubes are "capped." If the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2024· 3M Company - Health Care Business

Recalled Item: 3M Durapore Surgical Tape Recalled by 3M Company - Health Care Business Due...

The Issue: Select lots of the 3M Durapore Surgical Tape, Catalog Number 1538-118, were...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2024· Draeger Medical, Inc.

Recalled Item: Dr¿ger Perseus A500 Anesthesia Workstation Recalled by Draeger Medical, Inc....

The Issue: Unexpected shutdown while operating on battery power.

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

Class I — Serious Health HazardOngoing
DrugMarch 19, 2024· Pyramids Wholesale Inc.

Recalled Item: Weiner Boner Honey Recalled by Pyramids Wholesale Inc. Due to Undeclared...

The Issue: Marketed without an approved NDA/ANDA: Products found to contain undeclared...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugMarch 19, 2024· Pyramids Wholesale Inc.

Recalled Item: Flower Power Recalled by Pyramids Wholesale Inc. Due to Undeclared Sildenafil

The Issue: Marketed without an approved NDA/ANDA: Products found to contain undeclared...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugMarch 19, 2024· Pyramids Wholesale Inc.

Recalled Item: Pink Pussycat Honey Recalled by Pyramids Wholesale Inc. Due to Undeclared...

The Issue: Marketed without an approved NDA/ANDA: Products found to contain undeclared...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund