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Ceros
Rhino Medical Supply Inc · Model RM-SN15D · UDI-DI 00850060997457
KYW
Prescription
2
510(k) clearances
209
Adverse events
13
Recalls
216
Facilities
Description
Ceros Syringe Tip Cap, White, Polypropylene, Fits Luer Lock and Luer Slip, Covers entire luer port, Sterile Blister Pack, Latex Free
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2025-10-14 | Becton Dickinson & Company | BD has confirmed through internal testing that certain device trays failed routine biocompatibility testing. |
| 2024-05-09 | Sol-Millennium Medical Inc. | Products in distribution were found by FDA to be to be substantially different from the current cleared 510(k)s with a major change or modification to the device s intended use. |
| 2022-07-04 | Medicina Uk Ltd | Plunger component has been manufactured with an unapproved material (Polyethylene not Polypropylene) and does not meet raw material specification |
| 2022-07-04 | Medicina Uk Ltd | Plunger component has been manufactured with an unapproved material (Polyethylene not Polypropylene) and does not meet raw material specification |
| 2022-07-04 | Medicina Uk Ltd | Plunger component has been manufactured with an unapproved material (Polyethylene not Polypropylene) and does not meet raw material specification |
| 2022-07-04 | Medicina Uk Ltd | Plunger component has been manufactured with an unapproved material (Polyethylene not Polypropylene) and does not meet raw material specification |
| 2022-07-04 | Medicina Uk Ltd | Plunger component has been manufactured with an unapproved material (Polyethylene not Polypropylene) and does not meet raw material specification |
| 2022-07-04 | Medicina Uk Ltd | Plunger component has been manufactured with an unapproved material (Polyethylene not Polypropylene) and does not meet raw material specification |
| 2022-07-04 | Medicina Uk Ltd | Plunger component has been manufactured with an unapproved material (Polyethylene not Polypropylene) and does not meet raw material specification |
| 2022-07-04 | Medicina Uk Ltd | Plunger component has been manufactured with an unapproved material (Polyethylene not Polypropylene) and does not meet raw material specification |
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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.