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. 1,064 recalls have been distributed to Kansas in the last 12 months.

50,117 total recalls
1,064 in last 12 months

Showing 13121–13140 of 28,538 recalls

Medical DeviceAugust 19, 2019· CooperSurgical, Inc.

Recalled Item: LEEP Return Patient Pads (10/ box) Model # 6050Pl used Recalled by...

The Issue: Discrepancy between the correct expiration dates on the individual pouches...

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

Class III — Low RiskOngoing
Medical DeviceAugust 19, 2019· Howmedica Osteonics Corp.

Recalled Item: TRIATHLON FEMORAL DISTAL AUGMENT 10MM - SIZE 2 RIGHT Catalog Recalled by...

The Issue: Due to device overhang issue that protrudes beyond the medial periphery of...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2019· Becton, Dickinson and Company, BD Biosciences

Recalled Item: BD FACSLyric Flow Cytometer Recalled by Becton, Dickinson and Company, BD...

The Issue: Flow cytometers, when used with specific tubes may experience excessive...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2019· Becton, Dickinson and Company, BD Biosciences

Recalled Item: BD FACSLyric Flow Cytometer Recalled by Becton, Dickinson and Company, BD...

The Issue: Flow cytometers, when used with specific tubes may experience excessive...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2019· Howmedica Osteonics Corp.

Recalled Item: TRIATHLON FEMORAL DISTAL AUGMENT 10MM - SIZE 2 LEFT Catalog Recalled by...

The Issue: Due to device overhang issue that protrudes beyond the medial periphery of...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2019· Becton, Dickinson and Company, BD Biosciences

Recalled Item: BD FACSLyric Flow Cytometer Recalled by Becton, Dickinson and Company, BD...

The Issue: Flow cytometers, when used with specific tubes may experience excessive...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2019· Howmedica Osteonics Corp.

Recalled Item: TRIATHLON FEMORAL DISTAL AUGMENT 15MM - SIZE 2 LEFTTriathlon Femoral...

The Issue: Due to device overhang issue that protrudes beyond the medial periphery of...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2019· Howmedica Osteonics Corp.

Recalled Item: TRIATHLON FEMORAL DISTAL AUGMENT 15MM - SIZE 2 RIGHT Catalog Recalled by...

The Issue: Due to device overhang issue that protrudes beyond the medial periphery of...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2019· Becton, Dickinson and Company, BD Biosciences

Recalled Item: BD FACSLyric Flow Cytometer Recalled by Becton, Dickinson and Company, BD...

The Issue: Flow cytometers, when used with specific tubes may experience excessive...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2019· Becton, Dickinson and Company, BD Biosciences

Recalled Item: BD FACSLyric Flow Cytometer Recalled by Becton, Dickinson and Company, BD...

The Issue: Flow cytometers, when used with specific tubes may experience excessive...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2019· Becton, Dickinson and Company, BD Biosciences

Recalled Item: BD FACSLyric Flow Cytometer Recalled by Becton, Dickinson and Company, BD...

The Issue: Flow cytometers, when used with specific tubes may experience excessive...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2019· OrthoPediatrics Corp

Recalled Item: Model No. 01-1501-0032 (Child Nail Attachment Bolt). Component of the...

The Issue: Binding can occur between the attachment bolt and intramedullary nail, which...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2019· OrthoPediatrics Corp

Recalled Item: OrthoPediatrics Adolescent attachment bolt used with the Pediatric Nailing...

The Issue: Interference can occur between the adolescent attachment bolt and the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2019· OrthoPediatrics Corp

Recalled Item: Model No. 01-1503-0032 (Adolescent Nail Attachment Bolt). Component of the...

The Issue: Binding can occur between the attachment bolt and intramedullary nail, which...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2019· Becton, Dickinson and Company, BD Biosciences

Recalled Item: BD FACSLyric Flow Cytometer Recalled by Becton, Dickinson and Company, BD...

The Issue: Flow cytometers, when used with specific tubes may experience excessive...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2019· RESPIRATORY THERAPEUTICS GROUP LLC

Recalled Item: RespVent Closed Suction System T-Piece Tracheostomy Adult Recalled by...

The Issue: It has been determined that some units of catheters were not tightly...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2019· Intuitive Surgical, Inc.

Recalled Item: da Vinci SP Camera Recalled by Intuitive Surgical, Inc. Due to Some cameras...

The Issue: Some cameras were found to have residual soil adhered to the tip of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2019· IrriMAX Corporation

Recalled Item: Irrisept Wound Debridement and Cleansing System. 12 units per case. Recalled...

The Issue: Potential defect in the sterile pouch seal, which may result in a lack of...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2019· Normand-Info S.A.S.U.

Recalled Item: Remisol Advance running on hardware with Windows XP Recalled by Normand-Info...

The Issue: A patch was released for a critical remote code execution vulnerability in...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2019· Western / Scott Fetzer Company

Recalled Item: Grab n Go Opti series VIPR system Model # PRX-9627 Recalled by Western /...

The Issue: Limited access to flow settings as a result of the control knob having been...

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

Class II — Potential Health HazardOngoing