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. 1,705 recalls have been distributed to Kansas in the last 12 months.

50,117 total recalls
1,705 in last 12 months

Showing 4486144880 of 50,117 recalls

Medical DeviceAugust 30, 2013· Zimmer, Inc.

Recalled Item: Versys¿ Beaded Fullcoat Femoral Stem (POR FULL-CT FEM ST 11X160MM Recalled...

The Issue: The low density polyethylene (LDPE) bag used to package implants adheres to...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2013· Zimmer, Inc.

Recalled Item: Natural-Knee¿ II Femoral Component Recalled by Zimmer, Inc. Due to The low...

The Issue: The low density polyethylene (LDPE) bag used to package implants adheres to...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2013· CareFusion 303, Inc.

Recalled Item: SmartSite Low Sorbing Infusion Set Recalled by CareFusion 303, Inc. Due to...

The Issue: CareFusion is recalling the SmartSite Low Sorbing Infusion Set, Model#...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2013· GE Healthcare, LLC

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

The Issue: GE Healthcare has recently become aware of a potential safety issue...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2013· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance CT Big Bore Oncology Recalled by Philips Medical Systems...

The Issue: There are artifacts appearing on the Tracker images during...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2013· Stryker Endoscopy

Recalled Item: Stryker Vision Mounting Arm Recalled by Stryker Endoscopy Due to When...

The Issue: When positioning the display located on top of the video cart, it is...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2013· Implantech Associates Inc

Recalled Item: Device Name: Terino Square Chin-Style II-Medium Recalled by Implantech...

The Issue: Implantech initiated a voluntary recall of certain lots of Terino Square...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2013· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Emit 2000 Phenobarbital Assay and Syva Emit 2000 Phenobarbital Assay...

The Issue: Imprecision with certain lots

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2013· Zimmer, Inc.

Recalled Item: CoCr Head (Not distributed in the United States) Used in Recalled by Zimmer,...

The Issue: The low density polyethylene (LDPE) bag used to package implants adheres to...

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

Class II — Potential Health HazardOngoing
DrugAugust 30, 2013· Boehringer Ingelheim Roxane Inc

Recalled Item: SPIRIVA HandiHaler (Tiotropium Bromide Inhalation Powder) Capsules 18 mcg...

The Issue: Presence of Foreign Substance: This recall is being conducted due to the...

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

Class III — Low RiskOngoing
Refund
DrugAugust 30, 2013· Watson Laboratories Inc

Recalled Item: Hydrocodone Bitartrate and Acetaminophen Tablets Recalled by Watson...

The Issue: Defective Container: Defective bottles may not have tamper evident seals...

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

Class III — Low RiskOngoing
Refund
DrugAugust 30, 2013· Hospira Inc.

Recalled Item: Aminosyn II Recalled by Hospira Inc. Due to Presence of Particulate Matter:...

The Issue: Presence of Particulate Matter: Confirmed customer complaint of particulate...

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 29, 2013· Procter & Gamble Co

Recalled Item: Vicks NyQuil Cold and Flu Nighttime Relief Recalled by Procter & Gamble Co...

The Issue: Incorrect/ Undeclared Excipients: NyQuil Liquid Original bottles were...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 29, 2013· Cubist Pharmaceuticals, Inc.

Recalled Item: Cubicin (daptomycin for injection) Recalled by Cubist Pharmaceuticals, Inc....

The Issue: Presence of Particulate Matter; Glass particulates observed in vials

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 29, 2013· Dr. Reddy's Laboratories, Inc.

Recalled Item: IBU (TM) IBUPROFEN Tablets Recalled by Dr. Reddy's Laboratories, Inc. Due to...

The Issue: Labeling: Incorrect or missing lot and/or exp date- This product is being...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 29, 2013· Hospira Inc.

Recalled Item: 5% Lidocaine HCl and 7.5% Dextrose Injection Recalled by Hospira Inc. Due to...

The Issue: Presence of Particulate Matter; report of visible particulates in the glass...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 29, 2013· Fresenius Medical Care Holdings, Inc.

Recalled Item: 2008K@ Home Blood lines Combiset True Flow Series for Hemodialysis Recalled...

The Issue: Updated Instructions for Use: Bloodline connections not tightened per...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2013· Carestream Health Inc.

Recalled Item: Carestream DRX-Revolution Mobile X-Ray System -- Made in U.S.A. by Recalled...

The Issue: It was discovered that Carestream received a report from a customer that 2...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2013· DePuy Mitek, Inc., a Johnson & Johnson Co.

Recalled Item: DePuy Mitek FMS Intermediary Tubing with One-Way valve Product Code:...

The Issue: Pillow valve included in the FMS Duo outflow tubing set and the FMS Solo...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2013· Carestream Health Inc.

Recalled Item: DRX- Revolution Recalled by Carestream Health Inc. Due to Carestream Health...

The Issue: Carestream Health Inc. has conducted a voluntary field action which includes...

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

Class II — Potential Health HazardOngoing