BD Insyte Autoguard BC recall
BD Insyte Autoguard BC, Shielded IV Catheter with Blood Control Technology, REF: 382533, 20 GA x 1.00 in (1.1x25 mm) 63 mL/min, Rx Only. BD Insyte…
Why was BD Insyte Autoguard BC recalled?
Catheters may contain a hole in the catheter tubing, which could result in leakage during the insertion process.
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?
Lot # 4127714/ UDI-DI: 00382903825332
- Product
- BD Insyte Autoguard BC, Shielded IV Catheter with Blood Control Technology, REF: 382533, 20 GA x 1.00 in (1.1x25 mm) 63 mL/min, Rx Only. BD Insyte…
- Recalling firm
- Becton Dickinson Infusion Therapy Systems, Inc.
- Quantity
- 26,400 units
- Distribution
- US: IL OUS: N/A0
- Recall date
- August 7, 2024
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)