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. 2,334 recalls have been distributed to Kansas in the last 12 months.

50,117 total recalls
2,334 in last 12 months

Showing 4776147780 of 50,117 recalls

Medical DeviceNovember 10, 2012· Orthovita, Inc., dBA Stryker Orthobiologics.

Recalled Item: Stryker Orthobiologics Aliquot Delivery System Manual Surgical Instrument -...

The Issue: There have been a few reported cases of the catheter breaking when removing...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2012· Orthovita, Inc., dBA Stryker Orthobiologics.

Recalled Item: Stryker Orthobiologics Aliquot Delivery System Manual Surgical Instrument -...

The Issue: There have been a few reported cases of the catheter breaking when removing...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2012· Orthovita, Inc., dBA Stryker Orthobiologics.

Recalled Item: Stryker Orthobiologics Aliquot Delivery System Manual Surgical Instrument -...

The Issue: There have been a few reported cases of the catheter breaking when removing...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2012· Orthovita, Inc., dBA Stryker Orthobiologics.

Recalled Item: Stryker Orthobiologics Aliquot Delivery System Manual Surgical Instrument -...

The Issue: There have been a few reported cases of the catheter breaking when removing...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2012· Orthovita, Inc., dBA Stryker Orthobiologics.

Recalled Item: Stryker Orthobiologics Aliquot Delivery System Manual Surgical Instrument -...

The Issue: There have been a few reported cases of the catheter breaking when removing...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2012· Orthovita, Inc., dBA Stryker Orthobiologics.

Recalled Item: Stryker Orthobiologics Aliquot Delivery System Manual Surgical Instrument -...

The Issue: There have been a few reported cases of the catheter breaking when removing...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2012· Orthovita, Inc., dBA Stryker Orthobiologics.

Recalled Item: Stryker Orthobiologics Aliquot Delivery System Manual Surgical Instrument -...

The Issue: There have been a few reported cases of the catheter breaking when removing...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2012· Orthovita, Inc., dBA Stryker Orthobiologics.

Recalled Item: Stryker Orthobiologics Aliquot Delivery System Manual Surgical Instrument -...

The Issue: There have been a few reported cases of the catheter breaking when removing...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2012· Orthovita, Inc., dBA Stryker Orthobiologics.

Recalled Item: Stryker Orthobiologics Aliquot Delivery System Manual Surgical Instrument -...

The Issue: There have been a few reported cases of the catheter breaking when removing...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2012· Orthovita, Inc., dBA Stryker Orthobiologics.

Recalled Item: Stryker Orthobiologics Aliquot Delivery System Manual Surgical Instrument -...

The Issue: There have been a few reported cases of the catheter breaking when removing...

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

Class II — Potential Health HazardOngoing
DrugNovember 9, 2012· Ranbaxy Inc.

Recalled Item: Atorvastatin Calcium Tablets Recalled by Ranbaxy Inc. Due to Presence of...

The Issue: Presence of Particulate Matter: Certain batches of Atorvastatin tablets 10...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 9, 2012· Ranbaxy Inc.

Recalled Item: Atorvastatin Calcium Tablets Recalled by Ranbaxy Inc. Due to Presence of...

The Issue: Presence of Particulate Matter: Certain batches of Atorvastatin tablets 10...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 9, 2012· Ranbaxy Inc.

Recalled Item: Atorvastatin Calcium Tablets Recalled by Ranbaxy Inc. Due to Presence of...

The Issue: Presence of Particulate Matter: Certain batches of Atorvastatin tablets 10...

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 9, 2012· Frito Lay, Inc

Recalled Item: Grandma's Peanut Butter Mini Sandwich Creme Cookies Recalled by Frito Lay,...

The Issue: The firm is recalling GRANDMA'S Peanut Butter Sandwich Creme cookies and...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodNovember 9, 2012· Frito Lay, Inc

Recalled Item: Grandma's Peanut Butter Sandwich Creme Cookies Recalled by Frito Lay, Inc...

The Issue: The firm is recalling GRANDMA'S Peanut Butter Sandwich Creme cookies and...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
Medical DeviceNovember 9, 2012· Cooper Vision Caribbean Corp.

Recalled Item: AVAIRA (enfilcon A) Soft (Hydrophilic) Daily Wear Toric Contact Lenses...

The Issue: The lenses exceeded the acceptance limit for silicone oil residual.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 9, 2012· SpineFrontier, Inc.

Recalled Item: Drill Guide - Chameleon FacetFuse Fixation System Recalled by SpineFrontier,...

The Issue: Prior to use in surgery, the Drill Guides were presenting noticeable degrees...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 9, 2012· GE Healthcare, LLC

Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare became...

The Issue: GE Healthcare became aware of a potential issue associated with the LOGIQ e...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 9, 2012· Medtronic Neuromodulation

Recalled Item: SynchroMed EL Recalled by Medtronic Neuromodulation Due to Medtronic...

The Issue: Medtronic notified Healthcare Professionals of the impact of unapproved...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 9, 2012· Medtronic Neuromodulation

Recalled Item: Medtronic SynchroMed II Recalled by Medtronic Neuromodulation Due to...

The Issue: Medtronic notified Healthcare Professionals of the impact of unapproved...

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

Class I — Serious Health HazardOngoing