Home › 3M UNITEK CORPORATION › 3M™ Unitek™
3M™ Unitek™
3M UNITEK CORPORATION · Model 404-246 · UDI-DI 60652221303457
ECI
Prescription
10
510(k) clearances
18
Adverse events
3
Recalls
121
Facilities
Description
3M™ Unitek™ Elastics, 404-246, Medium-Light 3.5 oz, 5/16 in, Blue (Cliff), 100/Pk, 30 Pk/Ct
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2023-12-21 | G & H Wire Company | Latex elastic bands were labeled as non-latex elastic bands, an allergic rx can occur due to patient latex allergy |
| 2021-01-21 | G & H Wire Company | The text on the patient pack is correct and the product itself remains unchanged. FlexMedics does not expect device failures; Instead, there is an opportunity for misuse of the dev |
| 2011-08-18 | Biomet Microfixation, Inc. | On 09/18/2011, Biomet Microfixation, Jacksonville, FL, recalled their SP-2411, Rubber Band, Lot 307850 because it was labeled and sold as "LATEX FREE" although it contains "LATEX". |
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.
