Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-1470-2022 — Medline Convenience kits labeled as follows: a. BEDSIDE PICC CDS, Model Number CDS984642, b. VASCULAR CDS, Model Number DYNJ902880J, c. VASCULAR CDS, Model Number DYNJ902880K, d. OPEN HEART A & B, Model Number DYNJ904831F, e. OPEN HEART MHS, Model Number DYNJ905394A, f. OPEN HEART MHS, Model Number

U.S. FDA — Device Enforcement · United States · 2022-06-06 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-1470-2022
Date of alert: 2022-06-06
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: MEDLINE INDUSTRIES, LP - SPT
Product category: device
Product type: Devices

Reported risk: Kits contain leaking bottles of isopropyl alcohol

Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.

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