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. 2,630 recalls have been distributed to Nebraska in the last 12 months.
Showing 4401–4420 of 28,140 recalls
Recalled Item: Non-sterile convenience kits: Medline Open Heart CDS Recalled by MEDLINE...
The Issue: Surgical convenience kits containing Pure Pouch component that has weak...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Non-sterile convenience kits: a. Medline CC Drawer 4 IV Circulation Recalled...
The Issue: Surgical convenience kits containing Pure Pouch component that has weak...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile surgical convenience kit: Medline Neuro IR Pack Recalled by MEDLINE...
The Issue: Surgical convenience kits containing Pure Pouch component that has weak...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Non-sterile convenience kits: a. Medline Difficult Airway Tray W/O Cook...
The Issue: Surgical convenience kits containing Pure Pouch component that has weak...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile convenience kits: a. Medline Retrograde PK-22025203-LF Recalled by...
The Issue: Surgical convenience kits containing Pure Pouch component that has weak...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prelude Guide Sheath Roadster Recalled by Merit Medical Systems, Inc. Due to...
The Issue: Their is a potential that sheaths labeled with .018 dilators may contain a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Keller Funnel 2 Recalled by Allergan Sales, LLC Due to Their is a potential...
The Issue: Their is a potential that breast implants lack the lubricious coating that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: PIEZON Bottle Product Name: PIEZON Bottle Model/Catalog Number:...
The Issue: Received complaints that bottles assembled with one batch of bottle collars...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: CLEANER BOTTLE Product Name: CLEANER BOTTLE Model/Catalog...
The Issue: Received complaints that bottles assembled with one batch of bottle collars...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: WATER BOTTLE Product Name: WATER BOTTLE Model/Catalog Number:...
The Issue: Received complaints that bottles assembled with one batch of bottle collars...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vanguard Knee System AS Tibial Bearing / DCM ArCom Recalled by Biomet, Inc....
The Issue: Possible damage to the Vanguard Knee System AS Tibial Bearing caused during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BioZorb Marker-BioZorb 3D Bioabsorbable Marker-Intended Use radiographic...
The Issue: Safety Information: Complaints describe complications/adverse events that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica CH Iron3 - IVD use in the quantitative measurement Recalled by...
The Issue: Potential for falsely elevated Chol_2, LDLC, and Trig_2 results on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia 3.0T CX Recalled by Philips North America Llc Due to Patient support...
The Issue: Patient support table floor plate may be incorrectly installed.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ATTUNE AFFIXIUM Cementless Fixed Bearing Knee with 3DP Technology Recalled...
The Issue: Product incorrectly labelled.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia Elition X Recalled by Philips North America Llc Due to Patient...
The Issue: Patient support table floor plate may be incorrectly installed.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intera CV Recalled by Philips North America Llc Due to Patient support table...
The Issue: Patient support table floor plate may be incorrectly installed.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Achieva 1.5T Conversion Recalled by Philips North America Llc Due to Patient...
The Issue: Patient support table floor plate may be incorrectly installed.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intera 1.0T Power/Pulsar Recalled by Philips North America Llc Due to...
The Issue: Patient support table floor plate may be incorrectly installed.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Evolution Upgrade 3.0T Recalled by Philips North America Llc Due to Patient...
The Issue: Patient support table floor plate may be incorrectly installed.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.