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. 2,650 recalls have been distributed to Nebraska in the last 12 months.
Showing 2921–2940 of 49,150 recalls
Recalled Item: Monterey AL Implant Inserter Recalled by Stryker Spine Due to Potential for...
The Issue: Potential for the gold unlock button to separate from the inserter.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Neupogen (filgrastim) For Injection Recalled by Amgen, Inc. Due to Stability...
The Issue: Stability data does not support expiry: the products have the potential to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Neupogen (filgrastim) For Injection Recalled by Amgen, Inc. Due to Stability...
The Issue: Stability data does not support expiry: the products have the potential to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: t:slim X2 Insulin Pump with Interoperable Technology Recalled by Tandem...
The Issue: A software defect in Version 7.9 of the pump software for Tandem t:slim X2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tandem Mobi Insulin Pump with Interoperable Technology Recalled by Tandem...
The Issue: A software defect in Version 7.9 of the pump software for Tandem t:slim X2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Premier Solo Diamond - Large Invented Cone Recalled by Premier Dental...
The Issue: The hardness not meeting the material specification and may cause the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Names: MyDay Toric Recalled by CooperVision, Inc. Due to a limited...
The Issue: a limited number of lots were manufactured with an incorrect cylinder power.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NexGen LPS Flex Recalled by Zimmer, Inc. Due to The "Use with plate 7, 8, 9,...
The Issue: The "Use with plate 7, 8, 9, 10" compatibility statement on top of the label...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hippo 072 Aspiration System including Cheetah Delivery Tool and Aspiration...
The Issue: Aspiration catheter distal tip features and characteristics may not be in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DxC 500 AU Clinical Chemistry Analyzer Recalled by Beckman Coulter Inc. Due...
The Issue: Beckman Coulter has determined that device software versions V1.3, V1.4,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Da Vinci 5 Product Name: ASSY Recalled by Intuitive Surgical,...
The Issue: Due to an increase in complaints concerning foot tray pedal spring failing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: METFORMIN HYDROCHLORIDE EXTENDED- RELEASE 500MG Recalled by A-S Medication...
The Issue: Presence of Foreign Tablets/Capsules.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Prasugrel Tablets Recalled by MYLAN PHARMACEUTICALS INC Due to Failed...
The Issue: Failed Dissolution Specifications - low dissolution results
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Otopore Cylinder outer ear wound dressing Recalled by Stryker Corporation...
The Issue: There is a potential for blister seals on the product to present a bubble on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nasopore FD fragmentable nasal dressing Recalled by Stryker Corporation Due...
The Issue: There is a potential for blister seals on the product to present a bubble on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Otopore Square outer ear wound dressing Recalled by Stryker Corporation Due...
The Issue: There is a potential for blister seals on the product to present a bubble on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hemopore 8cm nasal/sinus temporary wound dressing Recalled by Stryker...
The Issue: There is a potential for blister seals on the product to present a bubble on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hemopore 2PK nasal/sinus temporary wound dressing Recalled by Stryker...
The Issue: There is a potential for blister seals on the product to present a bubble on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nasopore Standard 8cm fragmentable nasal dressing Recalled by Stryker...
The Issue: There is a potential for blister seals on the product to present a bubble on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nasopore 4cm Standard 2PK fragmentable nasal dressing Recalled by Stryker...
The Issue: There is a potential for blister seals on the product to present a bubble on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.