Home › CUTTING EDGE HC BRANDS LLC › Adapt O-Life
Adapt O-Life
CUTTING EDGE HC BRANDS LLC · Model RTG-07200 · UDI-DI 00853292007086
CAI
Prescription
10
510(k) clearances
2,368
Adverse events (11 deaths)
205
Recalls
201
Facilities
Description
Adapt O-Life Aerosol Tee Adapter Spring Loaded Valved 22mm O.D. x 22mm O.D. The Tee piece connector is designed for connecting to the patient port of the respiratory or anesthesia breathing circuit, or connecting nebulizer and corrugate tube or mouth piece.
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2026-08-11 | Medline Industries, LP | The kits contain certain lots of sterile applicators which may contain fungal contamination that may occur under certain environmental conditions, allowing the growth of Aspergillu |
| 2026-06-12 | Medline Industries, LP | The kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which have a potential breach of sterility in the packaging, due to wrinkles in the paper lidding whi |
| 2026-05-28 | Medline Industries, LP | Kits contain Swan-Ganz catheters recalled by Becton Dickinson (BD). BD has received complaints of leaks/breakage involving failures of the (blue) proximal injectate lumen hub on th |
| 2026-05-28 | Medline Industries, LP | Convenience Kits contain Covidien Mon-a-Therm General Purpose Temperature Probes Size 9 Fr. Medtronic has issued a recall of specific production lots of the Covidien Mon-a-Therm g |
| 2026-05-06 | Medline Industries, LP | The Medline Convenience Kits contain Arrow Kits and Sets that include Lidocaine Hydrochloride Injection, USP and Bupivacaine Hydrochloride in Dextrose Injection, USP which were rec |
| 2026-04-10 | Medline Industries, LP | Medline kits were distributed containing Huons Bupivacaine Hydrochloride in Dextrose Injection, USP, which was subsequently recalled due to quality issues, including microbiology t |
| 2026-03-19 | Medline Industries, LP | During 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 |
| 2026-02-16 | Medline Industries, LP | Kits contain recalled Olympus biopsy valves. Olympus is investigating an increase in complaints associated with rubber fragment detachment in the slit of single use biopsy valves. |
| 2026-01-07 | Medline Industries, LP | Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packag |
| 2026-01-07 | Medline Industries, LP | Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packag |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
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.
