Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Introcan Safety 3 Closed IV Catheter 22 Ga. x 1 in. Recalled by B Braun Medical Inc Due to Increased risk for valve housing detachment causing leakage.
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact B Braun Medical Inc directly.
Affected Products
Introcan Safety 3 Closed IV Catheter 22 Ga. x 1 in., PUR, Winged. Passive safety IV catheter.
Quantity: 28,200 units
Why Was This Recalled?
Increased risk for valve housing detachment causing leakage.
Where Was This Sold?
This product was distributed to 16 states: CA, FL, GA, IL, IN, MD, MN, MO, NM, NY, NC, PA, TN, TX, VA, WA
About B Braun Medical Inc
B Braun Medical Inc has 148 total recalls tracked by RecallDetector.
Related Recalls
EndoVive Safety PEG Kit Recalled by Boston Scientific Corporation Due to Recall of kits which utilized ChloraPrep Triple Swabsticks...
Boston Scientific Corporation · February 10, 2026
Owner's Booklets and Instructions for Use that are used with Recalled by Trividia Health, Inc. Due to The system labeling (user manual and online labeling)...
Trividia Health, Inc. · February 6, 2026
Artelon FlexBand Dynamic Matrix Ref: 31057 Recalled by International Life Sciences Due to Augmentation devices failed bacterial endotoxin testing.
International Life Sciences · February 6, 2026
Owner's Booklets and Instructions for Use that are used with Recalled by Trividia Health, Inc. Due to The system labeling (user manual and online labeling)...
Trividia Health, Inc. · February 6, 2026
Owner's Booklets and Instructions for Use that are used with Recalled by Trividia Health, Inc. Due to The system labeling (user manual and online labeling)...
Trividia Health, Inc. · February 6, 2026
Data sourced from the FDA (Device). Last updated March 26, 2026. View original report