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. 2,423 recalls have been distributed to Kansas in the last 12 months.
Showing 26221–26240 of 50,117 recalls
Recalled Item: BOX VATS1SCDX DO ZABIEGOW VATS Product Usage: The Endo GIA Recalled by...
The Issue: Device may be missing a sled component. The sled component is responsible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endo GIA" Auto Suture" Universal Articulating Loading Unit 30mm- 2.0mm...
The Issue: Device may be missing a sled component. The sled component is responsible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BOX1073076GASB1 BBR GASTRIC BYPASS S(Item Code BOX1073076GASB1 BBR GASTRIC...
The Issue: Device may be missing a sled component. The sled component is responsible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Convatec Esteem(TM) Synergy Stomahesive(R) Recalled by ConvaTec, Inc Due to...
The Issue: It was discovered that the stoma hole of one lots of the Esteem synergy...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE O.R. Necessities(TM) Sterile* Needle Counter Recalled by Medline...
The Issue: The product packaging seal has the potential to experience seal creep. This...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE O.R. Necessities(R) STERILE R Recalled by Medline Industries Inc Due...
The Issue: The product packaging seal has the potential to experience seal creep. This...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE Sterile* Needle Counter Recalled by Medline Industries Inc Due to...
The Issue: The product packaging seal has the potential to experience seal creep. This...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vulcan Fast Red Chromogen Kit 2 Recalled by Biocare Medical, LLC Due to...
The Issue: Chromogen failed to develop due to a stability issue caused by environmental...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE Sterile* Needle Counter Recalled by Medline Industries Inc Due to...
The Issue: The product packaging seal has the potential to experience seal creep. This...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE Sterile* Needle Counter Recalled by Medline Industries Inc Due to...
The Issue: The product packaging seal has the potential to experience seal creep. This...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE O.R. Necessities(TM) Sterile* Needle Counter Recalled by Medline...
The Issue: The product packaging seal has the potential to experience seal creep. This...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lean Pro 8 Cookies & Cream 1 Recalled by Labrada Nutrition, Inc Due to...
The Issue: Undeclared egg
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Lean Pro 8 Vanilla 2 Recalled by Labrada Nutrition, Inc Due to Undeclared Egg
The Issue: Undeclared egg
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Lean Pro 8 Chocolate 2 Recalled by Labrada Nutrition, Inc Due to Undeclared Egg
The Issue: Undeclared egg
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Metoprolol Succinate Extended-Release Tablets Recalled by Dr. Reddy's...
The Issue: Presence of Foreign Tablets/Capsules: One foreign tablet identified as...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Diltiazem HCl Extended-Release Capsules Recalled by Mckesson Packaging...
The Issue: Failed Dissolution Specifications. High dissolution results were obtained...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Diltiazem CD (Diltiazem Hydrochloride Extended-Release Capsules Recalled by...
The Issue: Failed Dissolution Specifications. High dissolution results were obtained...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Diltiazem HCl Extended-Release Capsules Recalled by Mckesson Packaging...
The Issue: Failed Dissolution Specifications. High dissolution results were obtained...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Diclofenac Sodium and Misoprostol Delayed Release Tablets 75 mg/0.2 mg...
The Issue: Labeling: Label Mix-Up: bottle labeled as Diclofenac Sodium and Misoprostol...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: LINX Management System Recalled by Torax Medical, Inc. Due to Possible out...
The Issue: Possible out of specification condition which may allow a bead component to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.