Oasis Medical, Inc. recalls HPMC Visoelastic, 8,000 cps, Reference 51082, LT5108 (Private Label), 2.0 mL in 3-mL Syringe, OASIS Medical Inc, 514 So…
- Recall date
- October 19, 2015
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- D-0524-2016
- FDA classification
- Class III
- Brand / firm
- Oasis Medical, Inc.
- Sold / distributed
- Nationwide and Saudi Arabia, Israel, Chile, Norway, Ecuador, Greece, Switzerland, Canada, England, Columbia, Poland, South Africa, Germany, Pakistan, El Salvador, Dubai, Belgium
Why it was recalled
Failed pH Specification: It has been determined that the pH of the lots recalled, may not meet specification at expiry.
Class III means the product violates regulations but is not likely to cause harm.
What was recalled
HPMC Visoelastic, 8,000 cps, Reference 51082, LT5108 (Private Label), 2.0 mL in 3-mL Syringe, OASIS Medical Inc, 514 South Vermont Avenue Glendora, CA 91741
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