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MEDLINE DYNJ04048Recalls & reported problems

Medline Industries, Inc. · KELLY FORCEPS/STD STR STERILE · Class 1

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. How this data works · Data updated Oct 13, 2026.

Recalls naming this device

  1. Nov 13, 2025Open, Classified

    The items may have weak packaging seals that may result in a breach of sterility if the seal fails and may lead to an increased risk of infection if product is utilized.

    Z-0922-2026 · Root cause: Packaging process control · FDA record ↗

  2. Feb 23, 2024Open, Classified

    Product may have a weak seal which may result in a breach of sterility of the contents if the seal fails. The weak seal may not be detectable by all users.

    Z-1437-2024 · Root cause: Process control · FDA record ↗

Other FORCEPS, GENERAL & PLASTIC SURGERY devices

All FORCEPS, GENERAL & PLASTIC SURGERY devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.