Drug recall
The BioZorb LP Marker is an implantable radiopaque marker used to facilitate visualization of a soft tissue…
FDA recall event 90734 · Class II · Hologic, Inc
Key facts
| Event ID | 90734 |
|---|---|
| Recall numbers | Z-1858-2022 |
| Recalling firm | Hologic, Inc |
| Product type | Devices |
| Products | The BioZorb LP Marker is an implantable radiopaque marker used to facilitate visualization of a soft tissue site. The BioZorb LP Marker is comprised of a bioabsorbable PLA (polylactic acid) component… |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Hologic BioZorb LP Marker, (Product number F0221), lot number 22A0RL, contained removable labels with an expiration date that indicated the product had already expired. The expiration date on the… |
| Initiation date | Aug 9, 2022 |
| Report date | Oct 12, 2022 |
| City | Marlborough |
| State | MA |
| Country | United States |
| FEI number | 1000120743 |
At a glance
- 1–9 Products in this recall
- 10–99 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: