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Snowden-Pencer
CAREFUSION 2200, INC · Model 89-8461 · UDI-DI 10885403067884
EBA
Prescription
1
510(k) clearances
15
Adverse events
5
Recalls
47
Facilities
Description
Snowden-Pencer MIS SNOWDEN-PENCER HEADLIGHT SYSTEM, ADJUSTABLE HEADBAND WITH 3.5MM X 9FT BIFURCATED FIBER OPTIC CABLE
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2025-07-03 | Orascoptic Surgical Acuity | Due to complaints, loupe nose pads containing nickel may cause an allergic reaction. |
| 2025-07-03 | Orascoptic Surgical Acuity | Due to complaints, loupe nose pads containing nickel may cause an allergic reaction. |
| 2025-07-03 | Orascoptic Surgical Acuity | Due to complaints, loupe nose pads containing nickel may cause an allergic reaction. |
| 2025-07-03 | Orascoptic Surgical Acuity | Due to complaints, loupe nose pads containing nickel may cause an allergic reaction. |
| 2011-11-17 | Kerr Corporation | The firm recalled the Freedom Cordless LED Headlight because some units were assembled with an incorrect component in the control board electronics that may cause some Freedom Cord |
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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.