FDA Device Intelligence
Home › Pemax Kunststoff GmbH › HMD cover set, consisting of 2 lens protective caps made of PP, color white

HMD cover set, consisting of 2 lens protective caps made of PP, color white

Pemax Kunststoff GmbH · Model 12741.12365 · UDI-DI 04260462740524

PUI Prescription
0
510(k) clearances
471
Adverse events
54
Recalls
398
Facilities

Description

HMD cover set, consisting of 2 lens protective caps made of PP, color white

Recalls

DateFirmReason
2026-09-09Medline Industries, LPReports of problems with product being difficult to remove from patient and leaving adhesive residue on patient's skin.
2026-09-09Medline Industries, LPReports of problems with product being difficult to remove from patient and leaving adhesive residue on patient's skin.
2026-09-09Medline Industries, LPReports of problems with product being difficult to remove from patient and leaving adhesive residue on patient's skin.
2026-09-09Medline Industries, LPReports of problems with product being difficult to remove from patient and leaving adhesive residue on patient's skin.
2026-09-09Medline Industries, LPReports of problems with product being difficult to remove from patient and leaving adhesive residue on patient's skin.
2026-09-09Medline Industries, LPReports of problems with product being difficult to remove from patient and leaving adhesive residue on patient's skin.
2026-09-09Medline Industries, LPReports of problems with product being difficult to remove from patient and leaving adhesive residue on patient's skin.
2026-09-09Medline Industries, LPReports of problems with product being difficult to remove from patient and leaving adhesive residue on patient's skin.
2026-09-09Medline Industries, LPReports of problems with product being difficult to remove from patient and leaving adhesive residue on patient's skin.
2026-09-09Medline Industries, LPReports 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 docs
Data 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.