REFRESH CONTACTS® Contact Lens Comfort Drops 91822USRecalls & reported problems
Allergan, Inc. · REFRESH CONTACTS® Contact Lens Comfort Drops · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- 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.
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
- Dec 29, 2020Class IITerminated
Missing Instruction For Use insert.
Z-0948-2021 · Root cause: Employee error · Recall details · FDA record ↗
Other Accessories, Soft Lens Products devices
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- Clear Care Clear Care 12ozAlcon Laboratories, Inc. · Accessories, soft lens products1 recall0 reports
- OPTI-FREE REPLENISH OPTI-FREE REPLENISH 2ozAlcon Laboratories, Inc. · Accessories, soft lens products1 recall0 reports
- OPTI-FREE REPLENISH OPTI-FREE REPLENISH 4ozAlcon Laboratories, Inc. · Accessories, soft lens products1 recall0 reports
- Clear Care Clear Care 2x12ozAlcon Laboratories, Inc. · Accessories, soft lens products4 reports
- Clear Care Clear Care 2x12ozAlcon Laboratories, Inc. · Accessories, soft lens products4 reports
- COMPLETE 93504LCAHZJohnson & Johnson Surgical Vision, Inc. · Accessories, soft lens products4 reports
- COMPLETE 93506LCAHZJohnson & Johnson Surgical Vision, Inc. · Accessories, soft lens products3 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026 · each recall links to the FDA recall notice
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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