Home › TIDI PRODUCTS, LLC › TIDIShield
TIDIShield
TIDI PRODUCTS, LLC · Model 5460 · UDI-DI 00618125142873
PUI
Prescription
0
510(k) clearances
471
Adverse events
54
Recalls
398
Facilities
Description
TIDIShield C-arm Equipment Covers Clear Kit Sterile Fits Siemens SIREMOBIL ISO-C & ARCADIS Orbic 20 per Case
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2026-09-09 | Medline Industries, LP | Reports of problems with product being difficult to remove from patient and leaving adhesive residue on patient's skin. |
| 2026-09-09 | Medline Industries, LP | Reports of problems with product being difficult to remove from patient and leaving adhesive residue on patient's skin. |
| 2026-09-09 | Medline Industries, LP | Reports of problems with product being difficult to remove from patient and leaving adhesive residue on patient's skin. |
| 2026-09-09 | Medline Industries, LP | Reports of problems with product being difficult to remove from patient and leaving adhesive residue on patient's skin. |
| 2026-09-09 | Medline Industries, LP | Reports of problems with product being difficult to remove from patient and leaving adhesive residue on patient's skin. |
| 2026-09-09 | Medline Industries, LP | Reports of problems with product being difficult to remove from patient and leaving adhesive residue on patient's skin. |
| 2026-09-09 | Medline Industries, LP | Reports of problems with product being difficult to remove from patient and leaving adhesive residue on patient's skin. |
| 2026-09-09 | Medline Industries, LP | Reports of problems with product being difficult to remove from patient and leaving adhesive residue on patient's skin. |
| 2026-09-09 | Medline Industries, LP | Reports of problems with product being difficult to remove from patient and leaving adhesive residue on patient's skin. |
| 2026-09-09 | Medline Industries, LP | Reports of problems with product being difficult to remove from patient and leaving adhesive residue on patient's skin. |
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.
