Home › MEDSAFETY SOLUTIONS LLC › KwikDose Oral Dispenser
KwikDose Oral Dispenser
MEDSAFETY SOLUTIONS LLC · Model 8105 · UDI-DI 00853832007262
KYX
Prescription
10
510(k) clearances
262
Adverse events (3 deaths)
17
Recalls
275
Facilities
Description
5 mL Amber KwikDose Pharmacy Pack, 100 count
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2024-03-04 | Avanos Medical, Inc. | The expiration date was not printed on the outer shipping label, leading to expired syringes being shipped to customers. |
| 2024-03-04 | Avanos Medical, Inc. | The expiration date was not printed on the outer shipping label, leading to expired syringes being shipped to customers. |
| 2024-03-04 | Avanos Medical, Inc. | The expiration date was not printed on the outer shipping label, leading to expired syringes being shipped to customers. |
| 2023-03-20 | Baxter Healthcare Corporation | ExataMed 20 mL oral dispenser component of the Clear Pharmacy Pack may have particulate matter. |
| 2022-07-22 | Baxter Healthcare Corporation | There is a potential of the packaging not maintaining a sterile barrier for the tip caps. |
| 2022-07-22 | Baxter Healthcare Corporation | There is a potential of the packaging not maintaining a sterile barrier for the tip caps. |
| 2022-07-22 | Baxter Healthcare Corporation | There is a potential of the packaging not maintaining a sterile barrier for the tip caps. |
| 2022-07-22 | Baxter Healthcare Corporation | There is a potential of the packaging not maintaining a sterile barrier for the tip caps. |
| 2022-07-22 | Baxter Healthcare Corporation | There is a potential of the packaging not maintaining a sterile barrier for the tip caps. |
| 2022-07-22 | Baxter Healthcare Corporation | There is a potential of the packaging not maintaining a sterile barrier for the tip caps. |
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.