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. 2,349 recalls have been distributed to Nebraska in the last 12 months.
Showing 2781–2800 of 28,140 recalls
Recalled Item: MEDLINE convenience kits labeled as: 1) ORAL SURGERY PK RFID Recalled by...
The Issue: Medline is recalling medical convenience manufactured using certain lots of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE convenience kits labeled as: 1) CLEAN CLOSING PACK Recalled by...
The Issue: Medline is recalling medical convenience manufactured using certain lots of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE convenience kits labeled as: 1) VAGINAL Recalled by MEDLINE...
The Issue: Medline is recalling medical convenience manufactured using certain lots of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE convenience kits labeled as: 1) LITHOTOMY/PELVISCOPY PACK Recalled...
The Issue: Medline is recalling medical convenience manufactured using certain lots of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE convenience kits labeled as: 1) MINOR EYE TRAY #81 Recalled by...
The Issue: Medline is recalling medical convenience manufactured using certain lots of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE convenience kits labeled as: 1) MAMMOPLASTY-LF Recalled by MEDLINE...
The Issue: Medline is recalling medical convenience manufactured using certain lots of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE convenience kits labeled as: 1) BREAST BIOPSY PACK-LF Recalled by...
The Issue: Medline is recalling medical convenience manufactured using certain lots of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE convenience kits labeled as: 1) GENERAL ENDOSCOPY PACK Recalled by...
The Issue: Medline is recalling medical convenience manufactured using certain lots of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SECURE 1000 mL EMPTY EVA CONTAINER With 2 Ports Recalled by The Metrix...
The Issue: A limited number of IV bags have been found to leak during filling.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Autosampler Recalled by Shimadzu Corp. Analytical & Measuring Instruments...
The Issue: There have been cases of failure of the main board due to condensation water...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MONOCRYL" (poliglecaprone 25) Suture MONOCRYL" Sutures are indicated...
The Issue: Due a component mix-up in manufacturing, the affected products may contain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Approach Hydro ST Micro Wire Guide Recalled by Cook Incorporated Due to...
The Issue: Affected device lots have labels that state the incorrect expiration dates.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Approach CTO Micro Wire Guide Recalled by Cook Incorporated Due to Affected...
The Issue: Affected device lots have labels that state the incorrect expiration dates.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trilogy EV300. Model Numbers: DS2200X11B Recalled by Philips Respironics,...
The Issue: Potential for in-line nebulizer configuration in certain locations to result...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trilogy Evo. Model Numbers: DS2110X11B Recalled by Philips Respironics, Inc....
The Issue: Potential for in-line nebulizer configuration in certain locations to result...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aeris EVO. Model Number: VT2110X24B. Intended for invasive and non-invasive...
The Issue: Potential for in-line nebulizer configuration in certain locations to result...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Garbin Evo. Model Number: LD2110X23B. Intended for invasive and non-invasive...
The Issue: Potential for in-line nebulizer configuration in certain locations to result...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DRG:HYBRiD-XL Insulin. Model/Catalog Number: HYE-5361 Recalled by DRG...
The Issue: The user of the assay may either face a failure message during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Zenition 70 Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due...
The Issue: Potential for the Mains Control Unit board fuse may blow out during system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Zenition 50 Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due...
The Issue: Potential for the Mains Control Unit board fuse may blow out during system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.