Facility
TOTAL TITANIUM, INC.
1 recall(s) on record — most severe on record: Class I.
| FDA Establishment Identifier (FEI) | 3007583964 |
|---|---|
| Establishment type | Remanufacture Medical Device; Manufacture Medical Device for Another Party (Contract Manufacturer); Manufacture Medical Device |
| Location | 281 Kennedy Drive Red Bud, IL, US 62278 |
| Registration status | Active · expires 2026 |
| Parent company | Bausch & Lomb Incorporated (owner-operator 9043551) |
Devices registered here (1)
- Spoon, OphthalmicProduct code HNB · Class I · Ophthalmic · 21 CFR 886.4350
Recalls & enforcement
- Class ITerminated2012-11-15Some disposable cannulas (with 4-digit lot numbers) provided with the Amvisc or Amvisc Plus OVD are not properly engaging to the Luer-Lock on the Amvisc and Amvisc Plus sterile glass syringes. The cannulas may leak viscoelastic material or detach from the syringe during injectio
Related
Source: U.S. FDA via openFDA (device registration & enforcement). Data as of 2026-08-13. Verify this facility record at FDA →
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