CODMAN 3000 Series recall
CODMAN 3000 Series Refill Set- Huber needles. Used in combination with the CODMAN 3000 Series Constant Flow Implantable Pump CATALOG NO. : AP-07014…
Why was CODMAN 3000 Series recalled?
Needle is leaking from hub/needle cannula connection
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 numbers: 14B114CT, 14E011CT, and 14E366CT
- Product
- CODMAN 3000 Series Refill Set- Huber needles. Used in combination with the CODMAN 3000 Series Constant Flow Implantable Pump CATALOG NO. : AP-07014…
- Recalling firm
- Codman & Shurtleff, Inc.
- Quantity
- 5463 units
- Distribution
- Worldwide Distribution-US (nationwide) and the countries of Canada, France, Germany, and Switzerland.
- Recall date
- June 3, 2015
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)