Product Recalls in Nebraska
Product recalls affecting Nebraska — including food, drugs, consumer products, medical devices, and vehicles distributed to Nebraska. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,868 recalls have been distributed to Nebraska in the last 12 months.
Showing 25941–25960 of 49,150 recalls
Recalled Item: (1) BOX BOX1073180 APPE1 APPENDIX KIT ZAMS (Item Code BOX1073180) Recalled...
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: 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: 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: 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(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 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(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 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: 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 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: 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: Alaris Infusion Pump administration sets labeled as: -Infusion Set Alaris...
The Issue: Complaints where users were unable to prime the administration set.
Recommended Action: Stop using. Contact the manufacturer or your 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.
Recalled Item: SOMATOM Go.Up Recalled by Siemens Medical Solutions USA, Inc Due to There is...
The Issue: There is a potential for a software issue that may cause the need for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.