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Robbins Microcannulas
Robbins Instruments Inc. · Model 21.CAN-FIC2250 · UDI-DI 90850010779303
2
510(k) clearances
74
Adverse events (2 deaths)
7
Recalls
82
Facilities
Description
Robbins Microcannulas 22Gx50mm
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2022-07-29 | Hobbs Medical, Inc. | Device label display an incorrect expiration date, extends the shelf life of the product. Affected product distributed in the United States from 3/25/2018 to 9/28/2020, expiration |
| 2015-01-23 | Biologic Therapies, Inc | Devices are misbranded - failure to properly classify and obtain FDA clearance prior distribution |
| 2015-01-23 | Biologic Therapies, Inc | Devices are misbranded - failure to properly classify and obtain FDA clearance prior distribution |
| 2015-01-23 | Biologic Therapies, Inc | Devices are misbranded - failure to properly classify and obtain FDA clearance prior distribution |
| 2013-11-26 | Becton Dickinson & Company | BD Interlink Threaded Lock Cannula REF# 303369 and lot #3021392 is being recalled due to the potential that a small percentage of the lot may exhibit open seals which adversely imp |
| 2013-05-14 | Maquet Cardiovascular Us Sales, Llc | The specified part numbers and lot numbers of Maquet Pediatric Arterial Cannula Packs may contain an incorrectly sized connector. |
| 2005-10-31 | Wilson-Cook Medical Inc | Misbranded; The catheter size listed on the product label is 6 French, which is inaccurate. The catheter size is more accurately described as 7 French. |
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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.