Home › Device types › KYW
Container, Liquid Medication, Graduated
FDA product code KYW · Class 1 · General Hospital
282
Registered devices
209
Adverse events
13
Recalls
2
510(k) clearances
Devices with this code
Monoject — Cardinal Health, Inc.BD Oral Syringe — BECTON, DICKINSON AND COMPANYHealth Care Logistics, Inc® — Health Care Logistics, Inc.BD Oral Syringe — BECTON, DICKINSON AND COMPANYMonoject — Cardinal Health 200, LLCMonoject — Cardinal Health 200, LLCHealth Care Logistics, Inc® — Health Care Logistics, Inc.Hayden Medical — Hayden Medical, Inc.Centurion — CENTURION MEDICAL PRODUCTS CORPORATIONHealth Care Logistics, Inc® — Health Care Logistics, Inc.Marina Medical — MARINA MEDICAL INSTRUMENTS, INC.Monoject — Cardinal Health, Inc.Bioseal Inc. — BIOSEALMonoject — Cardinal Health, Inc.BD Syringe Filling Connector — BECTON, DICKINSON AND COMPANYAvaline Medical NJ LLC — Avaline Medical NJ Limited Liability CompanyKangaroo — Cardinal Health, Inc.Monoject — Cardinal Health, Inc.MEDLINE — MEDLINE INDUSTRIES, INC.Health Care Logistics, Inc® — Health Care Logistics, Inc.Marina Medical — MARINA MEDICAL INSTRUMENTS, INC.CHS — Canadian Hospital Specialties LimitedMAXCRUSH — MAXPERT MEDICALBioseal Inc. — BIOSEAL
Recent 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 devic |
| 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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