Invasive Procedure Tray Mns9510 recall
INVASIVE PROCEDURE TRAY MNS9510
Why was Invasive Procedure Tray Mns9510 recalled?
Firm distributes kits which include the BD MaxZeroNeedleess Connector, which was recalled by the manufacturer due to the potential for droplets of fluid separating from the sealed surface of the connector following disconnection.
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?
2017100990 2017120490
- Product
- INVASIVE PROCEDURE TRAY MNS9510
- Recalling firm
- Centurion Medical Products Corporation
- Quantity
- 181965 total
- Distribution
- Nationwide domestic distribution.
- Recall date
- October 16, 2019
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)