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ARROW

TELEFLEX INCORPORATED · Model IPN042606 · UDI-DI 30801902128158

OGE Prescription
0
510(k) clearances
1,130
Adverse events
33
Recalls
35
Facilities

Description

Epidural Catheterization Kit with FlexTip Plus(R) Catheter FOR EXPORT ONLY

Recalls

DateFirmReason
2026-06-17Windstone Medical Packaging, Inc.Windstone Medical Packaging issued a recall for specific item(s) and lot(s) of Aligned Medical Solutions (AMS) convenience kits containing Elevaris Lidocaine HCl injection USP. El
2026-04-10Medline Industries, LPMedline kits were distributed containing Huons Bupivacaine Hydrochloride in Dextrose Injection, USP, which was subsequently recalled due to quality issues, including microbiology t
2026-03-19Medline Industries, LPDuring an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market product may be out-o
2026-01-29B Braun Medical IncB. Braun was notified by our supplier, Ferndale Laboratories, Inc., the manufacturer of MASTISOL Liquid Adhesive, that they have issued a voluntary recall due to potential crackin
2026-01-29B Braun Medical IncB. Braun was notified by our supplier, Ferndale Laboratories, Inc., the manufacturer of MASTISOL Liquid Adhesive, that they have issued a voluntary recall due to potential crackin
2026-01-29B Braun Medical IncB. Braun was notified by our supplier, Ferndale Laboratories, Inc., the manufacturer of MASTISOL Liquid Adhesive, that they have issued a voluntary recall due to potential crackin
2026-01-29B Braun Medical IncB. Braun was notified by our supplier, Ferndale Laboratories, Inc., the manufacturer of MASTISOL Liquid Adhesive, that they have issued a voluntary recall due to potential crackin
2025-09-18B BRAUN MEDICAL INCPotential for the lid of the catheter connector to be in the incorrect position.
2025-09-18B BRAUN MEDICAL INCPotential for the lid of the catheter connector to be in the incorrect position.
2025-09-18B BRAUN MEDICAL INCPotential for the lid of the catheter connector to be in the incorrect position.

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.