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Medline Industries, Inc. DYNJ82607Recalls & reported problems

Medline Industries, Inc. · SHOULDER REPAIR PACK-LF · Class 1

Data updated Oct 18, 2026 from official FDA records · Editorial policy

2 open recalls name this device. See the recall details and contact the manufacturer or your healthcare provider.

Adverse event reports
0
Deaths reported
0
Injuries reported
0
Recalls naming it
2

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. Oct 15, 2024Class IIOpen, Classified

    Some of the suture packages within the convenience kits contain the incorrect needle type/size and suture diameter/length.

    Z-0534-2025 · Root cause: Mixed-up of materials/components · Recall details · FDA record ↗

  2. Nov 17, 2022Class IIOpen, Classified

    Sterile blades within sterile kits have the potential for the blade to puncture the outer foil layer of the sterile packaging.

    Z-1096-2023 · Root cause: Device Design · Recall details · FDA record ↗

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Sources and updates

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