Medline custom medical procedure kits labeled as: DEEP recall: Endotoxin
Medline custom medical procedure kits labeled as: DEEP BRAIN STIMULATION PACK-LF
Why was Medline custom medical procedure kits labeled as: DEEP recalled?
Custom convenience kits are being recall because the contain non-sterile Codman Surgical Patties & Surgical Strips, which have the potential for endotoxin contamination.
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?
UDI/DI 10889942825547 (EA) 40889942825548 (CS), Lot Numbers: 19BKB326, 19DKA892, 19JDA775, 20ADC560
- Product
- Medline custom medical procedure kits labeled as: DEEP BRAIN STIMULATION PACK-LF
- Recalling firm
- MEDLINE INDUSTRIES, LP - Northfield
- Quantity
- 128 units
- Distribution
- Worldwide distribution - US Nationwide and the countries of UAE, and Canada.
- Recall date
- January 8, 2025
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)