Introcan Safety 3 Closed IV Catheter 22 Ga. x 1 in recall
Introcan Safety 3 Closed IV Catheter 22 Ga. x 1 in., PUR, Winged. Passive safety IV catheter.
Why was Introcan Safety 3 Closed IV Catheter 22 Ga. x 1 in recalled?
Increased risk for valve housing detachment causing leakage.
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?
Model No 4251128-02; UDI-DI 04046964014017; Lot 24F09G8952.
- Product
- Introcan Safety 3 Closed IV Catheter 22 Ga. x 1 in., PUR, Winged. Passive safety IV catheter.
- Recalling firm
- B Braun Medical Inc
- Quantity
- 28,200 units
- Distribution
- Domestic: CA, CA, FL, GA, IL, IL, IN, MD, MN, MO, NC, NM, NY, PA, TN, TX, VA, and WA; Foreign: Canada.
- Recall date
- March 26, 2025
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)