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. 2,420 recalls have been distributed to Kansas in the last 12 months.

50,117 total recalls
2,420 in last 12 months

Showing 3160131620 of 50,117 recalls

FoodNovember 23, 2016· Saputo Cheese USA, Inc.

Recalled Item: MOZZARELLA LOW MOISTURE WHOLE MILK 8/6# DRAGONE Recalled by Saputo Cheese...

The Issue: Firm received one complaint from a food service customer stating a...

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 23, 2016· Saputo Cheese USA, Inc.

Recalled Item: WHOLE MILK CHEESE 8/6# LA GONDOLA Recalled by Saputo Cheese USA, Inc. Due to...

The Issue: Firm received one complaint from a food service customer stating a...

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 23, 2016· Saputo Cheese USA, Inc.

Recalled Item: WHOLE MILK CHEESE 8/6# VESUVIO BELLA Recalled by Saputo Cheese USA, Inc. Due...

The Issue: Firm received one complaint from a food service customer stating a...

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 23, 2016· Saputo Cheese USA, Inc.

Recalled Item: WHOLE MILK CHEESE 8/6# MAGIC MOZZI Recalled by Saputo Cheese USA, Inc. Due...

The Issue: Firm received one complaint from a food service customer stating a...

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 23, 2016· NATURECOM INC

Recalled Item: DMAA (1 Recalled by NATURECOM INC Due to Naturecom dba NutriVitaShop is...

The Issue: Naturecom dba NutriVitaShop is recalling DMAA net weight 500 g because there...

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 23, 2016· Saputo Cheese USA, Inc.

Recalled Item: MOZZARELLA LOW MOISTURE WHOLE MILK 8/6# ROSELI Recalled by Saputo Cheese...

The Issue: Firm received one complaint from a food service customer stating a...

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 23, 2016· Saputo Cheese USA, Inc.

Recalled Item: MOZZARELLA SUPREME 8/6# CONTADINO Recalled by Saputo Cheese USA, Inc. Due to...

The Issue: Firm received one complaint from a food service customer stating a...

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 22, 2016· To Your Heart's Content

Recalled Item: Plush Puffs Marshmallows Toasty Coconut 4oz. and 2lb bulk bag Recalled by To...

The Issue: Undeclared allergen of milk from the declared ingredient coconut cream powder.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 22, 2016· Amendia, Inc

Recalled Item: Savannah-T Straight Rod Recalled by Amendia, Inc Due to The rods are...

The Issue: The rods are packaged in packages with unacceptable seals. In some cases,...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2016· Teleflex Medical

Recalled Item: RUSCH Recalled by Teleflex Medical Due to Labeling Inconsistency: The...

The Issue: Labeling Inconsistency: The products have been labeled with the incorrect...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2016· Siemens Healthcare Diagnostics, Inc.

Recalled Item: SIEMENS IMMULITE 2000/2000 Xpi Systems Intact PTH (Parathyroid Hormone) Test...

The Issue: Siemens is conducting this recall for the IMMULITE¿ 2000/IMMULITE¿ 2000 XPi...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2016· Amendia, Inc

Recalled Item: Black Widow 6.6mm x 20mm Screw Recalled by Amendia, Inc Due to There is a...

The Issue: There is a problem with the mating feature between the plate and screw which...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2016· Amendia, Inc

Recalled Item: Dual Stylet Needle Recalled by Amendia, Inc Due to The rods are packaged in...

The Issue: The rods are packaged in packages with unacceptable seals. In some cases,...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2016· Interventional Spine Inc

Recalled Item: G3 Opticage Expandable Interbody Fusion Device Recalled by Interventional...

The Issue: During implantation, the proximal end of the device could separate if the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2016· Amendia, Inc

Recalled Item: K-Wire 1.4mm x 12in Non-Threaded Recalled by Amendia, Inc Due to The rods...

The Issue: The rods are packaged in packages with unacceptable seals. In some cases,...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2016· Reckitt Benckiser LLC

Recalled Item: Durex Pleasure Pack . 3 ultra fine lubricated latex condoms Recalled by...

The Issue: Reckitt Benckiser LLC is recalling Durex Condoms Pleasure Packs due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2016· Amendia, Inc

Recalled Item: Black Widow Plate 19mm Plate Recalled by Amendia, Inc Due to There is a...

The Issue: There is a problem with the mating feature between the plate and screw which...

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

Class II — Potential Health HazardOngoing
DrugNovember 22, 2016· Les Emballages Knowlton Inc.

Recalled Item: Toms of Maine Naturally Dry Natural Powder Antiperspirant Stick Recalled by...

The Issue: Labeling: Label Mix Up- Incorrect back label applied to the product.

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

Class III — Low RiskOngoing
Refund
DrugNovember 22, 2016· Pfizer Inc.

Recalled Item: PROTONIX I.V. (pantoprazole sodium) for Injection Recalled by Pfizer Inc....

The Issue: Subpotent Drug: Out of Specification (OOS) for potency at the 6-month...

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

Class III — Low RiskOngoing
Refund
Medical DeviceNovember 21, 2016· GE Healthcare, LLC

Recalled Item: Prestilix Recalled by GE Healthcare, LLC Due to GE Healthcare is conducting...

The Issue: GE Healthcare is conducting a recall due to the potential fall of aged CRT...

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

Class II — Potential Health HazardOngoing