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. 2,636 recalls have been distributed to Kansas in the last 12 months.

50,117 total recalls
2,636 in last 12 months

Showing 31613180 of 50,117 recalls

Medical DeviceJanuary 31, 2025· Aesculap Inc

Recalled Item: Numerous models of nonsterile hemostatic forceps: (1) Recalled by Aesculap...

The Issue: The forceps have been used in ways not covered by the design resulting in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 31, 2025· GE Healthcare (China) Co., Ltd.

Recalled Item: SIGNA Creator Recalled by GE Healthcare (China) Co., Ltd. Due to For certain...

The Issue: For certain MR systems, a scan can be resumed following a Power Monitor trip...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 31, 2025· GE Healthcare (China) Co., Ltd.

Recalled Item: Optima MR360 Recalled by GE Healthcare (China) Co., Ltd. Due to For certain...

The Issue: For certain MR systems, a scan can be resumed following a Power Monitor trip...

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

Class II — Potential Health HazardOngoing
DrugJanuary 31, 2025· Alvogen, Inc

Recalled Item: Fentanyl Transdermal System CII Recalled by Alvogen, Inc Due to Defective...

The Issue: Defective delivery system - patches could be multi-stacked, adhered one on...

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

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 31, 2025· Nestle-USA, Inc. (Corporate Office)

Recalled Item: Gerber Snacks for Baby Soothe 'n' Chew TEETHING STICKS Banana Recalled by...

The Issue: Firm received complaints of infant choking.

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

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 31, 2025· Nestle-USA, Inc. (Corporate Office)

Recalled Item: Gerber Snacks for Baby Soothe 'n' Chew TEETHING STICKS Strawberry Recalled...

The Issue: Firm received complaints of infant choking.

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 30, 2025· The Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories

Recalled Item: Potassium Chloride Extended-Release Tablets Recalled by The Harvard Drug...

The Issue: Failed Dissolution Specifications.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 30, 2025· Micro Therapeutics, Inc.

Recalled Item: Medtronic Pipeline Vantage Embolization Device with Shield Technology...

The Issue: Use of embolization device with diameters greater-than-or-equal-to 4mm may...

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 30, 2025· Micro Therapeutics, Inc.

Recalled Item: Medtronic Pipeline Vantage Embolization Device with Shield Technology...

The Issue: Use of embolization device with diameters greater-than-or-equal-to 4mm may...

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 30, 2025· Telcare, LLC

Recalled Item: Philips Connected Blood Glucose Meter Recalled by Telcare, LLC Due to...

The Issue: Telcare, LLC has received customer complaints related to battery...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2025· LEICA BIOSYSTEMS NUSSLOCH GMBH

Recalled Item: Brand Name: Leica Biosystems Cryostats Product Name: CM1950 Model/Catalog...

The Issue: Firm became aware of software issues related to most recent firmware update...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 29, 2025· Pentax of America Inc

Recalled Item: Pentax Medical Video Processor- Intended to be used with PENTAX Recalled by...

The Issue: During endoscopic procedures using a combination of the video processor...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 29, 2025· Pentax of America Inc

Recalled Item: PENTAX Medical Video Colonoscope- Intended to provide optical visualization...

The Issue: During endoscopic procedures using a combination of the video processor...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 29, 2025· Pentax of America Inc

Recalled Item: PENTAX Medical Video Upper GI Scope-Intended to provide optical...

The Issue: During endoscopic procedures using a combination of the video processor...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 29, 2025· Stryker Corporation

Recalled Item: Stryker CinchLock Flex Knotless Anchor with Inserter and Suture Recalled by...

The Issue: Increase in complaints concerning "pullwire" breakage that may result in the...

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

Class II — Potential Health HazardOngoing
DrugJanuary 29, 2025· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Atomoxetine Capsules Recalled by Glenmark Pharmaceuticals Inc., USA Due to...

The Issue: CGMP Deviations: presence of N-Nitroso Atomoxetine Impurity above the FDA...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 29, 2025· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Atomoxetine Capsules Recalled by Glenmark Pharmaceuticals Inc., USA Due to...

The Issue: CGMP Deviations: presence of N-Nitroso Atomoxetine Impurity above the FDA...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 29, 2025· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Atomoxetine Capsules Recalled by Glenmark Pharmaceuticals Inc., USA Due to...

The Issue: CGMP Deviations: presence of N-Nitroso Atomoxetine Impurity above the FDA...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 29, 2025· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Atomoxetine Capsules Recalled by Glenmark Pharmaceuticals Inc., USA Due to...

The Issue: CGMP Deviations: presence of N-Nitroso Atomoxetine Impurity above the FDA...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 29, 2025· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Atomoxetine Capsules Recalled by Glenmark Pharmaceuticals Inc., USA Due to...

The Issue: CGMP Deviations: presence of N-Nitroso Atomoxetine Impurity above the FDA...

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

Class II — Potential Health HazardOngoing
Refund