Stimuplex A, 30 DEG, 21GX4", 0.80x100mm, Catalogue Number: 4894260
Reported: June 19, 2024 Initiated: May 17, 2024 #Z-2132-2024
Product Description
Stimuplex A, 30 DEG, 21GX4", 0.80x100mm, Catalogue Number: 4894260
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
- 1,783,991 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, 21GX4", 0.80x100mm, Catalogue Number: 4894260. Recalled by B Braun Medical Inc. Units affected: 1,783,991 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-2132-2024.
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