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. 1,805 recalls have been distributed to Kansas in the last 12 months.

50,117 total recalls
1,805 in last 12 months

Showing 3092130940 of 50,117 recalls

DrugFebruary 10, 2017· Synergy Rx

Recalled Item: RETINOIC ACID all strengths including 0.025% Recalled by Synergy Rx Due to...

The Issue: Lack of Assurance of Sterility: There are also CGMP Deviations.

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 10, 2017· Synergy Rx

Recalled Item: LIDOCAINE CREAM in all strengths including: 5% Recalled by Synergy Rx Due to...

The Issue: Lack of Assurance of Sterility: There are also CGMP Deviations.

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 10, 2017· Synergy Rx

Recalled Item: CLEAR (Benzoyl Peroxide 3.75% Recalled by Synergy Rx Due to Lack of...

The Issue: Lack of Assurance of Sterility: There are also CGMP Deviations.

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 10, 2017· Synergy Rx

Recalled Item: HI-LITE Cream (Retinoic Acid 0.05% Recalled by Synergy Rx Due to Lack of...

The Issue: Lack of Assurance of Sterility: There are also CGMP Deviations.

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 10, 2017· Synergy Rx

Recalled Item: MODIFIED JESSNER PEEL (Sal Acid 14% Recalled by Synergy Rx Due to Lack of...

The Issue: Lack of Assurance of Sterility: There are also CGMP Deviations.

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 10, 2017· Synergy Rx

Recalled Item: SUPREME CREAM (Retinoic acid 0.05% Recalled by Synergy Rx Due to Lack of...

The Issue: Lack of Assurance of Sterility: There are also CGMP Deviations.

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 10, 2017· Synergy Rx

Recalled Item: BICARBONATE 10% Recalled by Synergy Rx Due to Lack of Assurance of...

The Issue: Lack of Assurance of Sterility: There are also CGMP Deviations.

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 10, 2017· Synergy Rx

Recalled Item: ADAPALENE 0.1% Recalled by Synergy Rx Due to Lack of Assurance of Sterility:...

The Issue: Lack of Assurance of Sterility: There are also CGMP Deviations.

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 10, 2017· Synergy Rx

Recalled Item: RETINOIC ACID SOLUTION in all strengths including 0.3% Recalled by Synergy...

The Issue: Lack of Assurance of Sterility: There are also CGMP Deviations.

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 10, 2017· Synergy Rx

Recalled Item: TCA PEEL SOLUTION in all strengths including: 5% Recalled by Synergy Rx Due...

The Issue: Lack of Assurance of Sterility: There are also CGMP Deviations.

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 10, 2017· Sandoz Inc

Recalled Item: Pioglitazone and Glimepiride Tablets Recalled by Sandoz Inc Due to Failed...

The Issue: Failed Dissolution Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 10, 2017· Hospira Inc., A Pfizer Company

Recalled Item: METRONIDazole Injection Recalled by Hospira Inc., A Pfizer Company Due to...

The Issue: Lack of Sterility Assurance: customer report of leaking bag

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 10, 2017· Olympus Corporation of the Americas

Recalled Item: Olympus ENDOEYE HD II Video Telescopes Models: WA50040A Endoeye HD II...

The Issue: A damaged temperature sensor at the endoscope's tip can cause the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 9, 2017· Cardiovascular Systems Inc

Recalled Item: ViperWire Advance with Flextip Peripheral Atherectomy Guide Wire Recalled by...

The Issue: CSI is recalling three lots of VIPERWIRE ADVANCE WITH FLEXTIP PERIPHERAL...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 9, 2017· Remel Inc

Recalled Item: Remel Recalled by Remel Inc Due to Test organisms exhibit poor growth when...

The Issue: Test organisms exhibit poor growth when grown using the test agar. The poor...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2017· Medtronic

Recalled Item: SharkCore Fine Needle Biopsy System (22 GA) Recalled by Medtronic Due to...

The Issue: Handle may break during use.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2017· Del Mar Reynolds Medical, Ltd.

Recalled Item: Arkon Anesthesia Delivery System Recalled by Del Mar Reynolds Medical, Ltd....

The Issue: Spacelabs has received reports of the Arkon Anesthesia Delivery System,...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2017· Medtronic

Recalled Item: BNX Fine Need Aspiration System (19GA) Recalled by Medtronic Due to Handle...

The Issue: Handle may break during use.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2017· Medtronic

Recalled Item: SharkCore LG Fine Needle Biopsy System (19GA) Recalled by Medtronic Due to...

The Issue: Handle may break during use.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2017· Medtronic

Recalled Item: SharkCore Fine Needle Biopsy System (25GA) Recalled by Medtronic Due to...

The Issue: Handle may break during use.

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

Class II — Potential Health HazardOngoing