Medline custom medical procedure kits labeled as: 1) recall: Endotoxin
Medline custom medical procedure kits labeled as: 1) PANENDOSCOPY-LF, REF DYNJ36728C; 2) ENDOSCOPIC SINUS PACK, REF DYNJ40644A; 3) ENDO SINUS PACK…
Why was Medline custom medical procedure kits labeled as: 1) 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?
1) REF DYNJ36728C, UDI/DI 10193489265910(EA) (CS), Lot Numbers: 20EBK304, 20HBL260, 20LBA831, 20WBG513, 21DBK481, 21KBO816, 22BBJ543, 22FBD924, 22HBR956, 22KBJ095, 23BBF230, 23FBG752, 23HBI340, 23IBD038, 24CBG736, 24GBJ933; 2) REF DYNJ40644A, UDI/DI 10193489292176(EA) (CS), Lot Numbers: 20CMB952, 20HMB559, 20KMA468, 20KMB182, 20KMC866, 21AME524, 21DMA759, 21EME248, 21GMB592, 21HMC615, 21IMF418, 21JMA505, 21KMG859, 21LMF984; 3) REF DYNJ66449, UDI/DI 10193489356113(EA) (CS), Lot Numbers: 20EBN857, 20HBH423, 20HBN194.
- Product
- Medline custom medical procedure kits labeled as: 1) PANENDOSCOPY-LF, REF DYNJ36728C; 2) ENDOSCOPIC SINUS PACK, REF DYNJ40644A; 3) ENDO SINUS PACK…
- Recalling firm
- MEDLINE INDUSTRIES, LP - Northfield
- Quantity
- 1086 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)