Medline Industries, Inc. PAIN1470ARecalls & reported problems

Summary

No MAUDE adverse event reports in our data reference this device identifier directly.

2 FDA recall records name this device's identifier, 2 still open.

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

Recalls naming this device

1. May 21, 2026Class IIOpen, Classified

   The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for Lidocaine Ampules due to quality issues identified during a recent FDA manufacturing inspection of its drug manufacturing site.

   Z-2537-2026 · Root cause: Nonconforming Material/Component · Recall details · FDA record ↗

2. Oct 16, 2024Class IIOpen, Classified

   The connectors may not allow catheters to be inserted as intended if the connector is not in the fully open position.

   Z-0512-2025 · Root cause: Under Investigation by firm · Recall details · FDA record ↗