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HITACHI
HITACHI, LTD. · Model MP-2452-G16 · UDI-DI 04562122951685
OIJ
Prescription
0
510(k) clearances
1
Adverse events
2
Recalls
34
Facilities
Description
Puncture Guide Tube
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2017-07-07 | Hologic, Inc. | The firm is implementing a product correction involving its Affirm Lateral Arm Upright Biopsy Accessory, ASY-09880. The correction has been initiated due to a component (the Left-h |
| 2016-05-19 | Devicor Medical Products Inc | A 10 Gauge needle, 9cm long was shipped in an 8 Gauge needle, 15 cm package. |
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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.
