Medline procedural kits labeled as: NEURO TRAY recall
Medline procedural kits labeled as: NEURO TRAY, Pack Number DYNJ55909B
Why was Medline procedural kits labeled as: NEURO TRAY recalled?
Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/ other quality issues have been identified that may pose a risk to patient health.
What should I do if I have this product?
The recall is ongoing. Follow the firm and FDA instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
DYNJ55909B, Lot Number 23IBB122
- Product
- Medline procedural kits labeled as: NEURO TRAY, Pack Number DYNJ55909B
- Recalling firm
- MEDLINE INDUSTRIES, LP - Northfield
- Distribution
- Worldwide
- Recall date
- September 4, 2024
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)