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AutoSqueeze
OWEN MUMFORD USA INCORPORATED · Model OP 6100 · UDI-DI 00384706100012
1
510(k) clearances
1
Adverse events
2
Recalls
22
Facilities
Description
AutoSqueeze Eye Guide
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2023-03-30 | Apothecary Products, LLC | Potential for glass dropper to have glass particulate on the outside surface of the dropper bulb. |
| 2023-03-30 | Apothecary Products, LLC | Potential for glass dropper to have glass particulate on the outside surface of the dropper bulb. |
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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.