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. 924 recalls have been distributed to Kansas in the last 12 months.
Showing 48441–48460 of 50,117 recalls
Recalled Item: Hydrolyzed Whey Protein High Grade Recalled by MyoSci Technologies Inc. Due...
The Issue: True Nutrition is recalling Whey Protein Isolate, Whey Protein Concentrate,...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Whey Protein Isolate MicroFiltration Recalled by MyoSci Technologies Inc....
The Issue: True Nutrition is recalling Whey Protein Isolate, Whey Protein Concentrate,...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Whey Protein Isolate Cross-Flow Microfiltration Recalled by MyoSci...
The Issue: True Nutrition is recalling Whey Protein Isolate, Whey Protein Concentrate,...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Whey Protein Concentrate Recalled by MyoSci Technologies Inc. Due to...
The Issue: True Nutrition is recalling Whey Protein Isolate, Whey Protein Concentrate,...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Whey Protein Isolate Cold-Filtration Recalled by MyoSci Technologies Inc....
The Issue: True Nutrition is recalling Whey Protein Isolate, Whey Protein Concentrate,...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: The brand name is MRidium Series 1000 MR Infusion Sets Recalled by Iradimed...
The Issue: Iradimed Corporation is recalling MRidium Series 1000 MR Infusion Sets, Type...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MX 16-slice CT Scanner System Recalled by Philips Medical Systems...
The Issue: On August 24, 2012 the firm recalled the MX 16-slice after discovering that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optilock T15 AO Driver (3.5mm). Intended Use: The OptiLock Upper Recalled by...
The Issue: Field complaints indicate that recent shipments of the 14-400795 and 36505...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Universal Flex2 Breathing Circuit Class I 510(k) Exempt An anesthesia...
The Issue: King Systems received a customer complaint indicating that the customer had...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optilock 2.7 mm Screw Inserter. Intended Use: The OptiLock Upper Recalled by...
The Issue: Field complaints indicate that recent shipments of the 14-400795 and 36505...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mojo Nights Recalled by Evol Nutrition Due to Marketed Without an Approved...
The Issue: Marketed Without an Approved NDA/ANDA: The products were found to contain...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Novarel¿ (Chorionic Gonadotropin for injection Recalled by Ferring...
The Issue: Labeling; incorrect or missing insert; Warnings portion of the Package...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Mojo Nights for Her Recalled by Evol Nutrition Due to Marketed Without an...
The Issue: Marketed Without an Approved NDA/ANDA: The products were found to contain...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: S-Lift Implant Guides (also known as S-LIF) Compressor Part Number: Recalled...
The Issue: When using the optional S-LIFT (also known as S-LIF) Implant Guides without...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: S-Rom¿ Total Hip System Poly Liner Packaging: The insert is Recalled by...
The Issue: Orthopaedics, Inc. (DePuy) is issuing a voluntary recall of four lots of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dual Tip Marker Recalled by Viscot Medical LLC Due to Dual Tip Marker has...
The Issue: Dual Tip Marker has inconsistent ink flow on the black permanent ink side.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 12/14 TAPER HIGH OFFSET NECK USE WITH SMITH & NEPHEW Recalled by Smith &...
The Issue: Modular necks were manufactured out of specification by a vendor; the taper...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vycor Medical ViewSite Brain Access System 17mm/ 11mm / 5cm Recalled by...
The Issue: Vycor Medical recalled their VBAS (Vycor Viewsite Brain Access System)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ETHICON SURGIFLO HEMOSTATIC MATRIX Distributed by ETHICON ETHICON Recalled...
The Issue: SURGIFLO Hemostatic Matrix Kit & SURGIFLO Hemostatic Matrix Kit with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oxoid Antimicrobial Susceptibility Test Discs Recalled by Remel Inc Due to...
The Issue: The firm is recalling the product due to some cartridges may contain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.