Home › INTERNATIONAL FILTER PRODUCTS, INC. › International Filter Products, doing business as IFP Medical
International Filter Products, doing business as IFP Medical
INTERNATIONAL FILTER PRODUCTS, INC. · Model IFP-17G-0500 · UDI-DI 00860013851279
KPE
Prescription
10
510(k) clearances
6,805
Adverse events (8 deaths)
62
Recalls
85
Facilities
Description
Sterile Empty EVA Pillow Bag, 5000 mL, 3 Ports, With One LF Port
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2024-10-09 | The Metrix Company | A limited number of IV bags have been found to leak during filling. |
| 2024-10-09 | The Metrix Company | A limited number of IV bags have been found to leak during filling. |
| 2024-10-09 | The Metrix Company | A limited number of IV bags have been found to leak during filling. |
| 2024-10-09 | The Metrix Company | A limited number of IV bags have been found to leak during filling. |
| 2024-10-09 | The Metrix Company | A limited number of IV bags have been found to leak during filling. |
| 2024-10-09 | The Metrix Company | A limited number of IV bags have been found to leak during filling. |
| 2024-10-09 | The Metrix Company | A limited number of IV bags have been found to leak during filling. |
| 2024-10-09 | The Metrix Company | A limited number of IV bags have been found to leak during filling. |
| 2024-10-09 | The Metrix Company | A limited number of IV bags have been found to leak during filling. |
| 2024-10-09 | The Metrix Company | A limited number of IV bags have been found to leak during filling. |
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.