Bausch + Lomb BL5223WRecalls & reported problems
Bausch & Lomb Incorporated · TSV 23ga Posterior Vitrectomy Pack with Wide Field Illuminator · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 20
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 20 adverse event reports that list this exact device (DI 00757770058082), received between Oct 3, 2017 and Apr 5, 2019 — classified as 20 malfunctions.
The most frequently reported specific device problem is “Failure to Cut” (20 reports).
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.
Most reported problems
Device problems
- Failure to Cut20
Patient problems
- No Known Impact Or Consequence To Patient19
- No Consequences Or Impact To Patient18
Recent adverse event reports
The 20 most recent of 20 reports, in the reporter's own words as published by the FDA.
MalfunctionApr 5, 2019Failure to Cut; Failure to Cut
DURING A CATARACT SURGERY THE CUTTER DID NOT CUT HOWEVER IT CONTINUED TO ASPIRATE. THERE WAS NO PATIENT IMPACT.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 8487548 ↗MalfunctionFeb 8, 2019Failure to Cut; Failure to Cut
THE USER FACILITY IN (B)(6) REPORTED THE VITRECTOMY CUTTER COULD NOT CUT DURING SURGERY. ASPIRATION CONTINUED WHEN THE CUTTER STOPPED. THERE WAS NO IMPACT TO THE PATIENT.
Patient problems: No Consequences Or Impact To Patient; No Known Impact Or Consequence To Patient
MAUDE report 8321954 ↗MalfunctionFeb 8, 2019Failure to Cut; Failure to Cut
THE USER FACILITY IN (B)(6) REPORTED THE VITRECTOMY CUTTER COULD NOT CUT DURING SURGERY. ASPIRATION CONTINUED WHEN THE CUTTER STOPPED. THERE WAS NO IMPACT TO THE PATIENT.
Patient problems: No Consequences Or Impact To Patient; No Known Impact Or Consequence To Patient
MAUDE report 8321941 ↗MalfunctionFeb 8, 2019Failure to Cut; Failure to Cut
THE USER FACILITY IN (B)(6) REPORTED THE VITRECTOMY CUTTER COULD NOT CUT DURING SURGERY. ASPIRATION CONTINUED WHEN THE CUTTER STOPPED. THERE WAS NO IMPACT TO THE PATIENT.
Patient problems: No Consequences Or Impact To Patient; No Known Impact Or Consequence To Patient
MAUDE report 8321923 ↗MalfunctionFeb 8, 2019Failure to Cut; Failure to Cut
THE USER FACILITY IN (B)(6) REPORTED THE VITRECTOMY CUTTER COULD NOT CUT DURING SURGERY. ASPIRATION CONTINUED WHEN THE CUTTER STOPPED. THERE WAS NO IMPACT TO THE PATIENT.
Patient problems: No Consequences Or Impact To Patient; No Known Impact Or Consequence To Patient
MAUDE report 8321896 ↗MalfunctionFeb 8, 2019Failure to Cut; Failure to Cut
THE USER FACILITY IN (B)(6) REPORTED THE VITRECTOMY CUTTER COULD NOT CUT DURING SURGERY. ASPIRATION CONTINUED WHEN THE CUTTER STOPPED. THERE WAS NO IMPACT TO THE PATIENT.
Patient problems: No Consequences Or Impact To Patient; No Known Impact Or Consequence To Patient
MAUDE report 8321891 ↗MalfunctionFeb 7, 2019Failure to Cut; Failure to Cut
THE USER FACILITY IN (B)(6) REPORTED THE VITRECTOMY CUTTER COULD NOT CUT DURING SURGERY. ASPIRATION CONTINUED WHEN THE CUTTER STOPPED. THERE WAS NO IMPACT TO THE PATIENT.
Patient problems: No Consequences Or Impact To Patient; No Known Impact Or Consequence To Patient
MAUDE report 8317484 ↗MalfunctionFeb 6, 2019Failure to Cut; Failure to Cut
THE USER FACILITY IN (B)(6) REPORTED THE VITRECTOMY CUTTER COULD NOT CUT DURING SURGERY. ASPIRATION CONTINUED WHEN THE CUTTER STOPPED. THERE WAS NO IMPACT TO THE PATIENT.
Patient problems: No Consequences Or Impact To Patient; No Known Impact Or Consequence To Patient
MAUDE report 8312732 ↗MalfunctionFeb 6, 2019Failure to Cut; Failure to Cut
THE USER FACILITY IN (B)(4) REPORTED THE VITRECTOMY CUTTER COULD NOT CUT DURING SURGERY. ASPIRATION CONTINUED WHEN THE CUTTER STOPPED. THERE WAS NO IMPACT TO THE PATIENT.
Patient problems: No Consequences Or Impact To Patient; No Known Impact Or Consequence To Patient
MAUDE report 8312491 ↗MalfunctionFeb 6, 2019Failure to Cut; Failure to Cut
THE USER FACILITY IN (B)(4) REPORTED THE VITRECTOMY CUTTER COULD NOT CUT DURING SURGERY. ASPIRATION CONTINUED WHEN THE CUTTER STOPPED. THERE WAS NO IMPACT TO THE PATIENT.
Patient problems: No Consequences Or Impact To Patient; No Known Impact Or Consequence To Patient
MAUDE report 8312469 ↗MalfunctionFeb 6, 2019Failure to Cut; Failure to Cut
THE USER FACILITY IN (B)(6) REPORTED THE VITRECTOMY CUTTER COULD NOT CUT DURING SURGERY. ASPIRATION CONTINUED WHEN THE CUTTER STOPPED. THERE WAS NO IMPACT TO THE PATIENT.
Patient problems: No Consequences Or Impact To Patient; No Known Impact Or Consequence To Patient
MAUDE report 8312338 ↗MalfunctionFeb 6, 2019Failure to Cut; Failure to Cut
THE USER FACILITY IN (B)(6) REPORTED THE VITRECTOMY CUTTER COULD NOT CUT DURING SURGERY. ASPIRATION CONTINUED WHEN THE CUTTER STOPPED. THERE WAS NO IMPACT TO THE PATIENT.
Patient problems: No Consequences Or Impact To Patient; No Known Impact Or Consequence To Patient
MAUDE report 8312335 ↗MalfunctionFeb 6, 2019Failure to Cut; Failure to Cut
THE USER FACILITY IN (B)(6) REPORTED THE VITRECTOMY CUTTER COULD NOT CUT DURING SURGERY. ASPIRATION CONTINUED WHEN THE CUTTER STOPPED. THERE WAS NO IMPACT TO THE PATIENT.
Patient problems: No Consequences Or Impact To Patient; No Known Impact Or Consequence To Patient
MAUDE report 8312299 ↗MalfunctionFeb 6, 2019Failure to Cut; Failure to Cut
THE USER FACILITY IN (B)(6) REPORTED THE VITRECTOMY CUTTER COULD NOT CUT DURING SURGERY. ASPIRATION CONTINUED WHEN THE CUTTER STOPPED. THERE WAS NO IMPACT TO THE PATIENT.
Patient problems: No Consequences Or Impact To Patient; No Known Impact Or Consequence To Patient
MAUDE report 8312295 ↗MalfunctionFeb 6, 2019Failure to Cut; Failure to Cut
THE USER FACILITY IN (B)(6) REPORTED THE VITRECTOMY CUTTER COULD NOT CUT DURING SURGERY. ASPIRATION CONTINUED WHEN THE CUTTER STOPPED. THERE WAS NO IMPACT TO THE PATIENT.
Patient problems: No Consequences Or Impact To Patient; No Known Impact Or Consequence To Patient
MAUDE report 8312255 ↗MalfunctionFeb 6, 2019Failure to Cut; Failure to Cut
THE USER FACILITY IN (B)(6) REPORTED THE VITRECTOMY CUTTER COULD NOT CUT DURING SURGERY. ASPIRATION CONTINUED WHEN THE CUTTER STOPPED. THERE WAS NO IMPACT TO THE PATIENT.
Patient problems: No Consequences Or Impact To Patient; No Known Impact Or Consequence To Patient
MAUDE report 8312251 ↗MalfunctionFeb 6, 2019Failure to Cut; Failure to Cut
THE USER FACILITY IN (B)(6) REPORTED THE VITRECTOMY CUTTER COULD NOT CUT DURING SURGERY. ASPIRATION CONTINUED WHEN THE CUTTER STOPPED. THERE WAS NO IMPACT TO THE PATIENT.
Patient problems: No Consequences Or Impact To Patient; No Known Impact Or Consequence To Patient
MAUDE report 8312186 ↗MalfunctionFeb 6, 2019Failure to Cut; Failure to Cut
THE USER FACILITY IN (B)(6) REPORTED THE VITRECTOMY CUTTER COULD NOT CUT DURING SURGERY. ASPIRATION CONTINUED WHEN THE CUTTER STOPPED. THERE WAS NO IMPACT TO THE PATIENT.
Patient problems: No Consequences Or Impact To Patient; No Known Impact Or Consequence To Patient
MAUDE report 8312090 ↗MalfunctionJul 24, 2018Failure to Cut; Failure to Cut
DURING A CATARACT PROCEDURE THE VITRECTOMY CUTTER STOPPED CUTTING. A NEW PACK WAS OPENED TO CONTINUE THE SURGERY. NO PATIENT INJURY OR MEDICAL INTERVENTION WAS REQUIRED.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 7713452 ↗MalfunctionOct 3, 2017Failure to Cut; Failure to Cut
THE USER FACILITY IN (B)(4) REPORTED THE VITRECTOMY CUTTER HAD DIFFICULTY CUTTING. THERE WAS NO IMPACT TO THE PATIENT.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 6911599 ↗
Other Instrument, Vitreous Aspiration And Cutting, Ac-Powered devices
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- Ozil 8065750469Alcon Laboratories, Inc. · Instrument, vitreous aspiration and cutting, ac-powered261 reports
- Bausch + Lomb SE5523WVBausch & Lomb Incorporated · Instrument, Vitreous Aspiration And Cutting, Ac-Powered1 recall4 reports
- Infiniti 8065752160Alcon Laboratories, Inc. · Instrument, vitreous aspiration and cutting, ac-powered54 reports
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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 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- 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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