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. 2,616 recalls have been distributed to Kansas in the last 12 months.

50,117 total recalls
2,616 in last 12 months

Showing 49214940 of 28,538 recalls

Medical DeviceDecember 22, 2023· Onkos Surgical, Inc.

Recalled Item: ELEOS COLLAR STEM Recalled by Onkos Surgical, Inc. Due to Mislabeling

The Issue: Mislabeling of 13mm Modular Segmental Stem package (HC-13120-03M) which...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 22, 2023· Howmedica Osteonics Corp.

Recalled Item: HRIS ACET CUP CUT TIP 26X140 Part Number: 6210-5-100. single-use Recalled by...

The Issue: Failed to meet the acceptance criteria for the seal integrity and/or package...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 22, 2023· Howmedica Osteonics Corp.

Recalled Item: HRIS ACET CUP CUT TIP 32X140 Part Number: 6210-5-200rker. single-use...

The Issue: Failed to meet the acceptance criteria for the seal integrity and/or package...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 21, 2023· AMD Medicom Inc.

Recalled Item: PATTERSON¿ PROCEDURE EARLOOP MASKS- ANTI-FOG Recalled by AMD Medicom Inc....

The Issue: Level 3 masks were produced on alternate non-validated production equipment...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 21, 2023· AMD Medicom Inc.

Recalled Item: HENRY SCHEIN¿ CRITERION¿ EARLOOP MASKS LEVEL 3 (BLUE) (item code 570-2448)...

The Issue: Level 3 masks were produced on alternate non-validated production equipment...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 21, 2023· AMD Medicom Inc.

Recalled Item: HENRY SCHEIN¿ CRITERION¿ ANTI-FOG EARLOOP MASKS LEVEL 3 (BLUE) (item...

The Issue: Level 3 masks were produced on alternate non-validated production equipment...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 21, 2023· G & H Wire Company

Recalled Item: FLEXSelect 5/16" Amber Latex Elastics-Intended use is orthodontics Recalled...

The Issue: Latex elastic bands were labeled as non-latex elastic bands, an allergic rx...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 21, 2023· Ivoclar Vivadent, Inc.

Recalled Item: Article No. NA6050411 Recalled by Ivoclar Vivadent, Inc. Due to Affected...

The Issue: Affected product may not perform as expected; the amalgam powder may not...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 21, 2023· Covidien LP

Recalled Item: Surgilon Braided Nylon sutures: 88861919-31 SURGILON* 4-0 BLK 7X75CMPCT...

The Issue: Specific lots of sutures were sterilized with gamma doses that exceeded the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 21, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE BLOOD CULTURE KIT Recalled by MEDLINE INDUSTRIES, LP - Northfield...

The Issue: Medline Industries, LP is issuing a recall for specific item(s) and lot(s)...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 21, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE BLOOD CULTURE KIT Recalled by MEDLINE INDUSTRIES, LP - Northfield...

The Issue: Medline Industries, LP is issuing a recall for specific item(s) and lot(s)...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 21, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE BLOOD CULTURE COLLECTION KIT Recalled by MEDLINE INDUSTRIES, LP -...

The Issue: Medline Industries, LP is issuing a recall for specific item(s) and lot(s)...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 21, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE BLOOD CULTURE BOTTLE KIT Recalled by MEDLINE INDUSTRIES, LP -...

The Issue: Medline Industries, LP is issuing a recall for specific item(s) and lot(s)...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 21, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE ADULT BLOOD CULTURE KIT Recalled by MEDLINE INDUSTRIES, LP -...

The Issue: Medline Industries, LP is issuing a recall for specific item(s) and lot(s)...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 21, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE BLOOD CULTURE TRAY ADULT Recalled by MEDLINE INDUSTRIES, LP -...

The Issue: Medline Industries, LP is issuing a recall for specific item(s) and lot(s)...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 21, 2023· Covidien LP

Recalled Item: Sofsilk Braided Silk sutures: CS-211 SOFSILK* 4-0 BLK 45CM CVF21 Recalled by...

The Issue: Specific lots of sutures were sterilized with gamma doses that exceeded the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 21, 2023· MICROVENTION INC.

Recalled Item: TERUMO HydroPearl Compressible Microspheres for Embolisation Recalled by...

The Issue: Due to, during the manufacturing process, the prescribed manufacturing and...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 21, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE BLOOD CULTURE COLLECTION KIT Recalled by MEDLINE INDUSTRIES, LP -...

The Issue: Medline Industries, LP is issuing a recall for specific item(s) and lot(s)...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2023· Zyno Medical LLC

Recalled Item: Zyno Medical Z800 Large Volume Infusion Pumps -Intended to provide Recalled...

The Issue: When utlizing the patient query feature on the Zyno Medical Z-800WF pumps...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2023· CooperSurgical, Inc.

Recalled Item: global Medium Recalled by CooperSurgical, Inc. Due to The firm has become...

The Issue: The firm has become aware of a sudden increase in complaints for three...

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

Class II — Potential Health HazardOngoing