Hemo-Drop Blood Dispenser recall
Hemo-Drop Blood Dispenser, Part Number BMP-HEMODROP, used for preparing blood samples.
Why was Hemo-Drop Blood Dispenser recalled?
The metal cannula of the device either broke and the broken piece left in the blood specimen tube, or slid back into the plastic portion of the device instead of piercing the tube.
What should I do if I have this product?
Review the official FDA enforcement record for current 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?
UPC: (01) 20885380116008 Lot: 20180717A1
- Product
- Hemo-Drop Blood Dispenser, Part Number BMP-HEMODROP, used for preparing blood samples.
- Recalling firm
- Biomedical Polymers, Inc.
- Quantity
- 108,000
- Distribution
- US nationwide distribution.
- Recall date
- November 13, 2019
- Classification
- Class III
- Status
- Terminated
- Agency
- FDA (device)