Home › Dynarex Corporation › Resp-O2 Vortex 72 Closed Suction Tracheal Catheter, 16 FR (5.3 mm),30.5 cm/12 in
Resp-O2 Vortex 72 Closed Suction Tracheal Catheter, 16 FR (5.3 mm),30.5 cm/12 in
Dynarex Corporation · Model 31007 · UDI-DI 00840117344150
BSY
Prescription
10
510(k) clearances
3,474
Adverse events (42 deaths)
89
Recalls
248
Facilities
Description
T-Piece, Tracheal, Adult, STERILE-EO CONTENT: 1. Closed Suction Catheter (Adult), 1. MDI Adaptor, 1. 15 mm Swivel Adaptor, 1. 22 mm Flex Tube, 1. 15 mm x 22 mm Adaptor, 1. Trach Wedge, 1. Change of Day Sticker
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2025-03-19 | Avanos Medical, Inc. | Lack of sterility assurance for closed suction catheter systems |
| 2025-03-19 | Avanos Medical, Inc. | Lack of sterility assurance for closed suction catheter systems |
| 2025-03-19 | Avanos Medical, Inc. | Lack of sterility assurance for closed suction catheter systems |
| 2025-03-19 | Avanos Medical, Inc. | Lack of sterility assurance for closed suction catheter systems |
| 2025-03-19 | Avanos Medical, Inc. | Lack of sterility assurance for closed suction catheter systems |
| 2025-03-19 | Avanos Medical, Inc. | Lack of sterility assurance for closed suction catheter systems |
| 2025-03-19 | Avanos Medical, Inc. | Lack of sterility assurance for closed suction catheter systems |
| 2025-03-19 | Avanos Medical, Inc. | Lack of sterility assurance for closed suction catheter systems |
| 2024-04-08 | MEDLINE INDUSTRIES, LP - Northfield | Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/ other quality issues have been identified that ma |
| 2023-11-15 | MEDLINE INDUSTRIES, LP - Northfield | Medline Industries, LP is recalling certain kits and trays that were manufactured using specific lots of Nurse Assist (as components): 0.9% Sodium Chloride Irrigation USP, Sterile |
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Get your free API keyRead the docsData 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.