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BAUSCH and LOMB VAL038CTECBRecalls & reported problems

Medline Industries, Inc. · CATARACT PACK EYECARE CONSULT · Class 2

All models of BAUSCH and LOMB (6)

Data updated Oct 16, 2026 from official FDA records · Editorial policy

1 open recall names 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
1

Summary

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

1 FDA recall record name this device's identifier, 1 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 16, 2026.

Recalls naming this device

  1. Sep 4, 2024Class IIOpen, Classified

    It has been determined that certain Convenience kits that were packaged in breather pouch lot 323080002 may result in the potential of using non-sterile product if the vendor seal of the pouch is opened/unsealed.

    Z-0178-2025 · Root cause: Under Investigation by firm · Recall details · FDA record ↗

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Sources and updates

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