OriGen BIOMEDICAL VV13F Reinforced Dual Lumen Catheter recall
OriGen BIOMEDICAL VV13F Reinforced Dual Lumen Catheter STERILE DISPOSABLE: DO NOT RE-USE Manufactured by: OriGen Biomedical. OriGene VV13F Reinforced…
Why was OriGen BIOMEDICAL VV13F Reinforced Dual Lumen Catheter recalled?
Potential for clear extension tube to separate from the hub, which could result in blood loss and may require intervention to prevent permanent impairment/damage.
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?
Lot N18549
- Product
- OriGen BIOMEDICAL VV13F Reinforced Dual Lumen Catheter STERILE DISPOSABLE: DO NOT RE-USE Manufactured by: OriGen Biomedical. OriGene VV13F Reinforced…
- Recalling firm
- OriGen Biomedical, Inc.
- Quantity
- 51 units
- Distribution
- Worldwide Distribution: US (nationwide) and countries of: Spain, UK, Germany, Sweden, and Netherlands.
- Recall date
- April 29, 2015
- Classification
- Class I
- Status
- Terminated
- Agency
- FDA (device)