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Atellica® VTR Syringes

WESTMED, INC. · Model 11561343 · UDI-DI 00709078013348

JKA Prescription

510(k) clearances

49,665

Adverse events (3 deaths)

171

Recalls

221

Facilities

Description

1mL Vented Luer Slip Syringe, 25g x 5/8" Safety Tip, ~25IU Balanced Heparin, Vented Tip Cap (Private Label)

Recalls

Date	Firm	Reason
2026-07-29	Greiner Bio-One North America, Inc.	Lot B26043FM may include EDTA contamination which introduces potassium while chelating calcium in patient samples, leading to falsely elevated potassium (K+) and falsely decreased
2025-12-19	ICU Medical Inc.	Affected lots of syringes may have a crack on the syringe collar, which may lead to delayed or repeated blood draw/fluid delivery. This issue may also lead to blood leakage during
2025-09-26	ASP Global, LLC. dba Anatomy Supply Partners, LLC.	Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.
2025-09-26	ASP Global, LLC. dba Anatomy Supply Partners, LLC.	Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.
2025-09-26	ASP Global, LLC. dba Anatomy Supply Partners, LLC.	Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.
2025-09-26	ASP Global, LLC. dba Anatomy Supply Partners, LLC.	Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.
2025-09-26	ASP Global, LLC. dba Anatomy Supply Partners, LLC.	Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.
2025-09-26	ASP Global, LLC. dba Anatomy Supply Partners, LLC.	Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.
2025-09-26	ASP Global, LLC. dba Anatomy Supply Partners, LLC.	Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.
2025-09-26	ASP Global, LLC. dba Anatomy Supply Partners, LLC.	Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.

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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.