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ZYPREXA® Relprevv™ 405 mg Convenience Kit

ELI LILLY AND COMPANY · Model VL7637 · UDI-DI 00300027637112

FMI Prescription
10
510(k) clearances
39,876
Adverse events (68 deaths)
311
Recalls
449
Facilities

Description

Combination Drug/Device Convenience Kit: 1 - vial of Zyprexa Relprevv 405mg/vial (VL7637) 1 - 3 mL vial of Diluent 1 - 3 mL syringe w pre-attached Jelco 19-gauge 1.5 inch Hypodermic Needle-Pro need with needle protection device (EL31915 - GTIN 00351688072545) 2 - Jelco 19 gauge 1.5 inch Hypodermic Needle-Pro needles with needle protection device (EL1915 - GTIN 20351688075670)

Recalls

DateFirmReason
2026-07-30Bard Access Systems, Inc.After placement of intraosseous (IO) needle sets, used when intravenous access is difficult or impossible to obtain in emergent, urgent, or medically necessary cases, users may exp
2025-06-05Waismed Ltd.Due to manufacturing error, Intraosseous device built-in stabilizer may not be released properly after deployment and insertion.
2025-06-05Waismed Ltd.Due to manufacturing error, Intraosseous device built-in stabilizer may not be released properly after deployment and insertion.
2024-11-19Greiner Bio-One GmbHThe VACUETTE SAFELINK Holder with male luer lock may leak blood due to the protective rubber sleeve bunching up and not retracting when using the device.
2024-06-18Embecta Corp.BD Nano 2nd Gen Pen Needle was shipped close to or after the labeled expiration date of February 29, 2024. Using a device past its expiry sterility and integrity of the device cann
2024-02-05Retractable Technologies, Inc.The needle cannula of a retractable needle may detach from the needle holder in the patient.
2023-08-22Apellis Pharmaceuticals, Inc.19-gauge x 1" inch filter needles showed appearances of a small fraction of non-preferred characteristics. A causal relationship has not been established between the structural var
2023-07-26embecta Medical II LLCRetrospectively reported: Pen needles labeled 'For Investigational Use Only' were inadvertently distributed as commercially marketed devices.
2023-07-26embecta Medical II LLCRetrospectively reported: Pen needles labeled 'For Investigational Use Only' were inadvertently distributed as commercially marketed devices.
2022-06-20Bard Access Systems, Inc.BD Intraosseous Needle Kits may exhibit: 1) Increased force required to remove the stylet from intraosseous needle during placement may cause removal of the entire needle assembly

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Data 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.