Reported Jul 29, 2015 · Terminated
Bausch & Lomb SofPort Advanced Optics Aspheric Lens
Bausch & Lomb Surgical, Inc.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Bausch & Lomb Surgical, Inc. · 21 N Park Place Blvd · Clearwater, FL · 33759-3917
Is this the product you have?
- Bausch & Lomb SofPort Advanced Optics Aspheric Lens
- Lot codes and dates
- Produce CodeLI61AO and LI61SE. LOT #'s
1,039 of 1,039 codes
445550144557234456117445611844561234456207445621344562144456306445631644563184456319445640344564064456412445641344564144456415445641644567034456704445670744567104456711445671244567134456714445671544567164456717445671844567194456720445672144567224456723445672444567254456726445672744568014456803445680444568054456807445680844568094456810445681144568124456813445681444568154456816445681744568184456819445682044568214456822
- Produce CodeLI61AO and LI61SE. LOT #'s
- Amount recalled
- 72,773 units. 52,787 units (US) - 19,986 units (Foreign)
This recall covers 2 products
The agency filed one notice per product. You are reading one of them; the other one is below.
Where it was sold
Why it was recalled
Haptics breaking during lens loading and insertion.
This product could cause temporary or reversible health problems — stop using it.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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