BAUSCH and LOMBRecalls & reported problems across all models
Medline Industries, Inc. · 6 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
2 open recalls name at least one BAUSCH and LOMB model. Check whether yours is affected in the recall details, and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls
- 2
We found 6 models of BAUSCH and LOMB by Medline Industries, Inc. in the FDA's device registry (GUDID). Together they are named in 1 adverse event report in the FDA's MAUDE database, received between Jul 1, 2024 and Jul 1, 2024 — classified as 1 malfunction.
The most frequently reported specific device problem is “Crack” (1 report).
2 FDA recall records name at least one of these models by its device 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. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works
Reports received per month, all models
BAUSCH and LOMB recalls
FDA recall records that name at least one of these models by its device identifier, newest first. Each recall usually covers specific models or lots, so check the details.
- Sep 4, 2024Open, 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-0180-2025 · Root cause: Under Investigation by firm · Recall details · FDA record ↗
- Sep 4, 2024Open, 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 · names 5 of these models · Recall details · FDA record ↗
Most reported BAUSCH and LOMB problems
Device problems
- Crack1
- Material Integrity Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
BAUSCH and LOMB models
6 models, most reported first. Each model has its own page with its reports, recalls and device details.
- BAUSCH and LOMB LYN036EPESBOrthopedic tray1 recall1 report
- BAUSCH and LOMB LYN042CPFEGEye tray1 recall0 reports
- BAUSCH and LOMB LYN011PHNHDEye tray1 recall0 reports
- BAUSCH and LOMB LYN023BPSSDEye tray1 recall0 reports
- BAUSCH and LOMB VAL022BSOMDEye tray1 recall0 reports
- BAUSCH and LOMB VAL038CTECBEye tray1 recall0 reports
Recent BAUSCH and LOMB adverse event reports
The 1 most recent reports across all models, in the reporter's own words as published by the FDA.
MalfunctionJul 1, 2024Crack; Material Integrity Problem; Crack; Material Integrity Problem
Other Medline Industries, Inc. products
- Centurion Medical Products Corp52 models · 10 reports · 32 recalls
- NAMIC667 models · 229 reports · 22 recalls
- CURAD85 models · 295 reports · 4 recalls
- HUDSON RCI30 models · 190 reports · 2 recalls
- Excelsior8 models · 47 reports · 3 recalls
- Medline ReNewal18 models · 34 reports · 1 recall
- Guardian15 models · 77 reports
- MEDLINE UNITE10 models · 9 reports · 1 recall
Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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