Adlt Blood Culture Collect KIT recall
ADLT BLOOD CULTURE COLLECT KIT, REF DYNDH1245
Why was Adlt Blood Culture Collect KIT recalled?
This recall is being issued due to items within the kit have expired prior to the overall kit expiration date listed on the insert.
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 40889942604723 (case), 10889942604722 (unit): Lot Numbers: 23EMI373, 23EMF712, 23DMF155, 23CMH026
- Product
- ADLT BLOOD CULTURE COLLECT KIT, REF DYNDH1245
- Recalling firm
- MEDLINE INDUSTRIES, LP - Northfield
- Quantity
- 4850 kits
- Distribution
- US Nationwide distribution in the state of California.
- Recall date
- November 22, 2023
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)