Drug recall
(1) VitreQ 20G BF Blunt Needles-Ref: BF20.D51 GTIN: 8719214221089 (2) VitreQ 20G BF Brush Needles-REF…
FDA recall event 84661 · Class II · Vitreq Bv
Key facts
| Event ID | 84661 |
|---|---|
| Recall numbers | Z-0846-2020, Z-0847-2020, Z-0848-2020, Z-0849-2020, Z-0850-2020, Z-0851-2020, Z-0852-2020, Z-0853-2020, Z-0854-2020, Z-0855-2020, Z-0856-2020, Z-0857-2020 and 4 more |
| Recalling firm | Vitreq Bv |
| Product type | Devices |
| Products | (1) VitreQ 20G BF Blunt Needles-Ref: BF20.D51 GTIN: 8719214221089 (2) VitreQ 20G BF Brush Needles-REF: BF20.D52 GTIN: 8719214221102, (1) VitreQ 23G BF Blunt Needles-BF23.D51 GTIN#: 8719214221126 (2) VitreQ 23G BF Brush Needles-BF23.D52 GTIN#: 8719214221140, (1)VitreQ 25G BF Blunt Needles-BF25.D51 GITN: 8719214221164 (2) VitreQ 25G BF Brush Needles-BF25.D52 GTIN: 8719214221188, VitreQ 20G VFI Cannula-REF: CN20.D03 GTIN: 8719214221485, VitreQ 23G Blunt Needles with luer-lock connector-REF: CN23.D05 GTIN: 8719214221621 and 11 more |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Microscopic tears of the sterile pouch may compromise sterility |
| Initiation date | Dec 17, 2019 |
| Report date | Feb 5, 2020 |
| Termination date | Dec 9, 2020 |
| City | Vierpolders |
| Country | Netherlands |
| FEI number | 3012037425 |
At a glance
- 10–99 Products in this recall
- None 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: