Home › Amico Patient Care Corporation › Amico Patient Care Corporation
Amico Patient Care Corporation
Amico Patient Care Corporation · Model SSD-NI · UDI-DI 07540200000323
KDP
Prescription
10
510(k) clearances
99
Adverse events (6 deaths)
4
Recalls
29
Facilities
Description
SENTINEL VACUUM REGULATOR, DIGITAL, NEO INTERMITTENT, 0 - 100MMHG
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2018-03-12 | Ohio Medical Corporation | Final quality control testing was not completed before the devices were distributed.. |
| 2005-08-01 | Boehringer Laboratories, Inc. | Condition exists that prevents complete shutoff of the valve |
| 2005-08-01 | Boehringer Laboratories, Inc. | Condition exists that prevents complete shutoff of the valve |
| 2005-08-01 | Boehringer Laboratories, Inc. | Condition exists that prevents complete shutoff of the valve |
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 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.