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Sterile equipment drape
Spiggle & Theis Medizintechnik GmbH · Model 2565100GL · UDI-DI 04250676723277
PUI
Prescription
0
510(k) clearances
471
Adverse events
54
Recalls
398
Facilities
Description
for Zeiss microscopes HQ glass lens, Ø 65 mm, 5 pieces / box
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. |
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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.
