Drug recall
Bausch and Lomb 27G sterile cannula packed in the Bausch and Lomb Amvisc 1.2% Sodium Hyaluronate ( Model…
FDA recall event 63698 · Class I · Bausch and Lomb, Incorporated
Key facts
| Event ID | 63698 |
|---|---|
| Recall numbers | Z-0672-2013 |
| Recalling firm | Bausch and Lomb, Incorporated |
| Product type | Devices |
| Products | Bausch and Lomb 27G sterile cannula packed in the Bausch and Lomb Amvisc 1.2% Sodium Hyaluronate ( Model 59051, 59081, 59051L, 59081L) and Amvisc Plus 1.6% Sodium Hyaluronate (Model 60081, 60051… |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Some 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… |
| Initiation date | Nov 15, 2012 |
| Report date | Jan 23, 2013 |
| Termination date | Dec 4, 2013 |
| City | Aliso Viejo |
| State | CA |
| Country | United States |
| FEI number | 3004343135 |
At a glance
- 1–9 Products in this recall
- 1–9 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: