Medline Blood Cluture KIT recall
MEDLINE BLOOD CLUTURE KIT, Reorder #: DYNDH1592
Why was Medline Blood Cluture KIT recalled?
Adult Blood Culture Collect kit and Pre-Op Changing Bathing Kit contain an incorrect expiration date on a component with the kit. CHG Solution with the Pre-Op Changing Bathing Kit and Bactec bottle plastic both have an expiration date that does not match the date listed on the kit.
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 (01)40193489497220 (case), (01)10193489497229 (kit), Lot Numbers: 22GME974, 22FMF309
- Product
- MEDLINE BLOOD CLUTURE KIT, Reorder #: DYNDH1592
- Recalling firm
- MEDLINE INDUSTRIES, LP - Northfield
- Quantity
- 1600 kits
- Distribution
- US Nationwide distribution in the state of California.
- Recall date
- November 2, 2022
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)