PlainRecalls
FDA Devices Moderate Class II Ongoing

Stimuplex A, 30 DEG, 24GX1", 0.55x25mm, Catalogue Number: 4894251.

Reported: June 19, 2024 Initiated: May 17, 2024 #Z-2131-2024

Product Description

Stimuplex A, 30 DEG, 24GX1", 0.55x25mm, Catalogue Number: 4894251.

Reason for Recall

The devices are labeled "not made with DEHP" or the DEHP free symbol; however, the glue used contains traces of DEHP.

Details

Recalling Firm
B Braun Medical Inc
Units Affected
20,850 units
Distribution
Worldwide distribution - US Nationwide and the country of Canada.
Location
Breinigsville, PA

Frequently Asked Questions

What product was recalled?
Stimuplex A, 30 DEG, 24GX1", 0.55x25mm, Catalogue Number: 4894251.. Recalled by B Braun Medical Inc. Units affected: 20,850 units.
Why was this product recalled?
The devices are labeled "not made with DEHP" or the DEHP free symbol; however, the glue used contains traces of DEHP.
Which agency issued this recall?
This recall was issued by the FDA Devices on June 19, 2024. Severity: Moderate. Recall number: Z-2131-2024.