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. 2,413 recalls have been distributed to Kansas in the last 12 months.
Showing 33041–33060 of 50,117 recalls
Recalled Item: 100% Organic Spelt Flour Recalled by Montana Flour & Grains, Inc Due to...
The Issue: Organic Spelt Flour is recalled because label does not declare wheat.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Krusteaz Blueberry Pancake Mix Recalled by Continental Mills (Corporate...
The Issue: Krusteaz Blueberry Pancake Mix is recalled due to a potential to be...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Bulk packaged flour based "breader" packaged in 25 Recalled by Newly Weds...
The Issue: The supplier received flour from General Mills that was contaminated with E....
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Bulk packaged flour based tortilla bits packaged in 45.5 lb. bags. Recalled...
The Issue: The supplier received flour from General Mills that was contaminated with E....
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Artis zee/ zeego Recalled by Siemens Medical Solutions USA, Inc Due to Due...
The Issue: Due to an error in the 19 Live Display, image reproduction may fail in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper with release R8.2: Allura Xper FD10 Recalled by Philips...
The Issue: Increase in the failure rate of certain low-voltage DC power supplies ( DCPS )
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UNIQ 1.0: UNIQ FD10 Recalled by Philips Electronics North America...
The Issue: Increase in the failure rate of certain low-voltage DC power supplies (DCPS)
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Walrus Arterial Embolectomy Catheter The arterial embolectomy catheter is...
The Issue: Arrow is recalling due to incorrect labeling of products.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The TM Ardis Interbody System implant is a convex Recalled by Zimmer...
The Issue: This field action is being initiated following the firm's discovery of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Neptune Plus (Hemostatic Pad) Recalled by TZ Medical, Inc. Due to Neptune...
The Issue: Neptune Plus was mis-labeled and included the statement WITH ANTIMICROBIAL...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SPHERICAL HEAD (R) 6.5 MM CANCELLOUS SCREW Recalled by Smith & Nephew, Inc....
The Issue: The labels correctly state that the product should be a 25mm screw, but the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard TruGuide Disposable Coaxial Biopsy Needle Mixed Product Part Recalled...
The Issue: May contain two trocar tip stylets with coaxials or two blunt tip stylets...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RePlant¿ Angled Abutment Part Number 6050-52-60 Recalled by Implant Direct...
The Issue: Issue with design specification; oversized condition.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens RAPIDPoint¿ 500 v2.2.2A Software Upgrade Kit Recalled by Siemens...
The Issue: Some v2.2.2 upgrade kits include a dialysate mode which not cleared/approved...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AmediCheck Instant Test Cup Recalled by Branan Medical Corporation Due to...
The Issue: Branan Medical is recalling the AmediCheck Instant Test Cup, a 5 panel drug...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bulk flour bland breader packaged into 15 Recalled by Newly Weds Foods Inc...
The Issue: Flour contaminated with E. coli O121 was used in the manufacuring of flour...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Oxygen Nasal Wash (purified water Recalled by Let's Talk Health, Inc. Due to...
The Issue: Marketed Without An Approved NDA/ANDA: product is an unapproved drug due to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Zimmer¿ Air Dermatome II Width Plate Recalled by Zimmer Surgical Inc Due to...
The Issue: The surface coating applied to the device is blistering, peeling and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer¿ Air Dermatome II Width Plate Recalled by Zimmer Surgical Inc Due to...
The Issue: The surface coating applied to the device is blistering, peeling and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer¿ Air Dermatome II Width Plate Recalled by Zimmer Surgical Inc Due to...
The Issue: The surface coating applied to the device is blistering, peeling and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.