AcrySof IQ PanOptix Toric Trifocal IOLRecalls & reported problems across all models
Alcon Laboratories, Inc. · 165 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 336
- Deaths reported
- 0
- Injuries reported
- 248
- Recalls
- 0
We found 165 models of AcrySof IQ PanOptix Toric Trifocal IOL by Alcon Laboratories, Inc. in the FDA's device registry (GUDID). Together they are named in 336 adverse event reports in the FDA's MAUDE database, received between May 21, 2020 and Sep 11, 2026 — classified as 248 injuries, 88 malfunctions.
The most frequently reported specific device problem is “Device Dislodged or Dislocated” (24 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. 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
Most reported AcrySof IQ PanOptix Toric Trifocal IOL problems
Device problems
- Adverse Event Without Identified Device or Use Problem192
- Device Dislodged or Dislocated24
- Scratched Material24
- Appropriate Device Problem Term/Code Not Available16
- Defective Device16
- Crack12
- Malposition of Device12
- Break11
Patient problems
- Blurred Vision123
- Visual Impairment109
- Visual Disturbances94
- Halo52
- Insufficient Information50
- No Clinical Signs, Symptoms or Conditions36
- Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available32
- Dry Eye(s)12
AcrySof IQ PanOptix Toric Trifocal IOL models
165 models, 100 per page, most reported first. Each model has its own page with its reports, recalls and device details.
- AcrySof® IQ PanOptix® Toric Trifocal IOL TFNT30Lens, multifocal intraocular11 reports
- AcrySof® IQ PanOptix® Toric Trifocal IOL TFNT30Lens, multifocal intraocular8 reports
- AcrySof® IQ PanOptix® Toric Trifocal IOL TFNT30Lens, multifocal intraocular8 reports
- AcrySof® IQ PanOptix® Toric Trifocal IOL TFNT30Lens, multifocal intraocular7 reports
- AcrySof® IQ PanOptix® Toric Trifocal IOL TFNT30Lens, multifocal intraocular7 reports
- AcrySof® IQ PanOptix® Toric Trifocal IOL TFNT30Lens, multifocal intraocular7 reports
- AcrySof® IQ PanOptix® Toric Trifocal IOL TFNT30Lens, multifocal intraocular7 reports
- AcrySof® IQ PanOptix® Toric Trifocal IOL TFNT40Lens, multifocal intraocular7 reports
- AcrySof® IQ PanOptix® Toric Trifocal IOL TFNT30Lens, multifocal intraocular6 reports
- AcrySof® IQ PanOptix® Toric Trifocal IOL TFNT30Lens, multifocal intraocular6 reports
- AcrySof® IQ PanOptix® Toric Trifocal IOL TFNT30Lens, multifocal intraocular5 reports
- AcrySof® IQ PanOptix® Toric Trifocal IOL TFNT30Lens, multifocal intraocular5 reports
- AcrySof® IQ PanOptix® Toric Trifocal IOL TFNT40Lens, multifocal intraocular5 reports
- AcrySof® IQ PanOptix® Toric Trifocal IOL TFNT40Lens, multifocal intraocular5 reports
- AcrySof® IQ PanOptix® Toric Trifocal IOL TFNT30Lens, multifocal intraocular5 reports
- AcrySof® IQ PanOptix® Toric Trifocal IOL TFNT30Lens, multifocal intraocular5 reports
- AcrySof® IQ PanOptix® Toric Trifocal IOL TFNT40Lens, multifocal intraocular5 reports
- AcrySof® IQ PanOptix® Toric Trifocal IOL TFNT40Lens, multifocal intraocular4 reports
- AcrySof® IQ PanOptix® Toric Trifocal IOL TFNT30Lens, multifocal intraocular4 reports
- AcrySof® IQ PanOptix® Toric Trifocal IOL TFNT30Lens, multifocal intraocular4 reports
- AcrySof® IQ PanOptix® Toric Trifocal IOL TFNT30Lens, multifocal intraocular4 reports
- AcrySof® IQ PanOptix® Toric Trifocal IOL TFNT40Lens, multifocal intraocular4 reports
- AcrySof® IQ PanOptix® Toric Trifocal IOL TFNT30Lens, multifocal intraocular3 reports
- AcrySof® IQ PanOptix® Toric Trifocal IOL TFNT40Lens, multifocal intraocular3 reports
- AcrySof® IQ PanOptix® Toric Trifocal IOL TFNT40Lens, multifocal intraocular3 reports
- AcrySof® IQ PanOptix® Toric Trifocal IOL TFNT40Lens, multifocal intraocular3 reports
- AcrySof® IQ PanOptix® Toric Trifocal IOL TFNT40Lens, multifocal intraocular3 reports
- AcrySof® IQ PanOptix® Toric Trifocal IOL TFNT30Lens, multifocal intraocular3 reports
- AcrySof® IQ PanOptix® Toric Trifocal IOL TFNT30Lens, multifocal intraocular3 reports
- AcrySof® IQ PanOptix® Toric Trifocal IOL TFNT30Lens, multifocal intraocular3 reports
- AcrySof® IQ PanOptix® Toric Trifocal IOL TFNT30Lens, multifocal intraocular3 reports
- AcrySof® IQ PanOptix® Toric Trifocal IOL TFNT30Lens, multifocal intraocular3 reports
- AcrySof® IQ PanOptix® Toric Trifocal IOL TFNT30Lens, multifocal intraocular3 reports
- AcrySof® IQ PanOptix® Toric Trifocal IOL TFNT40Lens, multifocal intraocular3 reports
- AcrySof® IQ PanOptix® Toric Trifocal IOL TFNT40Lens, multifocal intraocular3 reports
- AcrySof® IQ PanOptix® Toric Trifocal IOL TFNT40Lens, multifocal intraocular3 reports
- AcrySof® IQ PanOptix® Toric Trifocal IOL TFNT40Lens, multifocal intraocular3 reports
- AcrySof® IQ PanOptix® Toric Trifocal IOL TFNT50Lens, multifocal intraocular3 reports
- AcrySof® IQ PanOptix® Toric Trifocal IOL TFNT60Lens, multifocal intraocular3 reports
- AcrySof® IQ PanOptix® Toric Trifocal IOL TFNT30Lens, multifocal intraocular2 reports
- AcrySof® IQ PanOptix® Toric Trifocal IOL TFNT30Lens, multifocal intraocular2 reports
- AcrySof® IQ PanOptix® Toric Trifocal IOL TFNT30Lens, multifocal intraocular2 reports
- AcrySof® IQ PanOptix® Toric Trifocal IOL TFNT30Lens, multifocal intraocular2 reports
- AcrySof® IQ PanOptix® Toric Trifocal IOL TFNT40Lens, multifocal intraocular2 reports
- AcrySof® IQ PanOptix® Toric Trifocal IOL TFNT40Lens, multifocal intraocular2 reports
- AcrySof® IQ PanOptix® Toric Trifocal IOL TFNT40Lens, multifocal intraocular2 reports
- AcrySof® IQ PanOptix® Toric Trifocal IOL TFNT40Lens, multifocal intraocular2 reports
- AcrySof® IQ PanOptix® Toric Trifocal IOL TFNT40Lens, multifocal intraocular2 reports
- AcrySof® IQ PanOptix® Toric Trifocal IOL TFNT40Lens, multifocal intraocular2 reports
- AcrySof® IQ PanOptix® Toric Trifocal IOL TFNT50Lens, multifocal intraocular2 reports
- AcrySof® IQ PanOptix® Toric Trifocal IOL TFNT50Lens, multifocal intraocular2 reports
- AcrySof® IQ PanOptix® Toric Trifocal IOL TFNT60Lens, multifocal intraocular2 reports
- AcrySof® IQ PanOptix® Toric Trifocal IOL TFNT60Lens, multifocal intraocular2 reports
- AcrySof® IQ PanOptix® Toric Trifocal IOL TFNT30Lens, multifocal intraocular2 reports
- AcrySof® IQ PanOptix® Toric Trifocal IOL TFNT30Lens, multifocal intraocular2 reports
- AcrySof® IQ PanOptix® Toric Trifocal IOL TFNT30Lens, multifocal intraocular2 reports
- AcrySof® IQ PanOptix® Toric Trifocal IOL TFNT30Lens, multifocal intraocular2 reports
- AcrySof® IQ PanOptix® Toric Trifocal IOL TFNT30Lens, multifocal intraocular2 reports
- AcrySof® IQ PanOptix® Toric Trifocal IOL TFNT30Lens, multifocal intraocular2 reports
- AcrySof® IQ PanOptix® Toric Trifocal IOL TFNT30Lens, multifocal intraocular2 reports
- AcrySof® IQ PanOptix® Toric Trifocal IOL TFNT40Lens, multifocal intraocular2 reports
- AcrySof® IQ PanOptix® Toric Trifocal IOL TFNT40Lens, multifocal intraocular2 reports
- AcrySof® IQ PanOptix® Toric Trifocal IOL TFNT40Lens, multifocal intraocular2 reports
- AcrySof® IQ PanOptix® Toric Trifocal IOL TFNT40Lens, multifocal intraocular2 reports
- AcrySof® IQ PanOptix® Toric Trifocal IOL TFNT40Lens, multifocal intraocular2 reports
- AcrySof® IQ PanOptix® Toric Trifocal IOL TFNT50Lens, multifocal intraocular2 reports
- AcrySof® IQ PanOptix® Toric Trifocal IOL TFNT50Lens, multifocal intraocular2 reports
- AcrySof® IQ PanOptix® Toric Trifocal IOL TFNT50Lens, multifocal intraocular2 reports
- AcrySof® IQ PanOptix® Toric Trifocal IOL TFNT60Lens, multifocal intraocular2 reports
- AcrySof® IQ PanOptix® Toric Trifocal IOL TFNT30Lens, multifocal intraocular1 report
- AcrySof® IQ PanOptix® Toric Trifocal IOL TFNT30Lens, multifocal intraocular1 report
- AcrySof® IQ PanOptix® Toric Trifocal IOL TFNT30Lens, multifocal intraocular1 report
- AcrySof® IQ PanOptix® Toric Trifocal IOL TFNT30Lens, multifocal intraocular1 report
- AcrySof® IQ PanOptix® Toric Trifocal IOL TFNT30Lens, multifocal intraocular1 report
- AcrySof® IQ PanOptix® Toric Trifocal IOL TFNT30Lens, multifocal intraocular1 report
- AcrySof® IQ PanOptix® Toric Trifocal IOL TFNT30Lens, multifocal intraocular1 report
- AcrySof® IQ PanOptix® Toric Trifocal IOL TFNT30Lens, multifocal intraocular1 report
- AcrySof® IQ PanOptix® Toric Trifocal IOL TFNT30Lens, multifocal intraocular1 report
- AcrySof® IQ PanOptix® Toric Trifocal IOL TFNT30Lens, multifocal intraocular1 report
- AcrySof® IQ PanOptix® Toric Trifocal IOL TFNT30Lens, multifocal intraocular1 report
- AcrySof® IQ PanOptix® Toric Trifocal IOL TFNT30Lens, multifocal intraocular1 report
- AcrySof® IQ PanOptix® Toric Trifocal IOL TFNT30Lens, multifocal intraocular1 report
- AcrySof® IQ PanOptix® Toric Trifocal IOL TFNT30Lens, multifocal intraocular1 report
- AcrySof® IQ PanOptix® Toric Trifocal IOL TFNT30Lens, multifocal intraocular1 report
- AcrySof® IQ PanOptix® Toric Trifocal IOL TFNT30Lens, multifocal intraocular1 report
- AcrySof® IQ PanOptix® Toric Trifocal IOL TFNT30Lens, multifocal intraocular1 report
- AcrySof® IQ PanOptix® Toric Trifocal IOL TFNT40Lens, multifocal intraocular1 report
- AcrySof® IQ PanOptix® Toric Trifocal IOL TFNT40Lens, multifocal intraocular1 report
- AcrySof® IQ PanOptix® Toric Trifocal IOL TFNT40Lens, multifocal intraocular1 report
- AcrySof® IQ PanOptix® Toric Trifocal IOL TFNT40Lens, multifocal intraocular1 report
- AcrySof® IQ PanOptix® Toric Trifocal IOL TFNT40Lens, multifocal intraocular1 report
- AcrySof® IQ PanOptix® Toric Trifocal IOL TFNT40Lens, multifocal intraocular1 report
- AcrySof® IQ PanOptix® Toric Trifocal IOL TFNT40Lens, multifocal intraocular1 report
- AcrySof® IQ PanOptix® Toric Trifocal IOL TFNT40Lens, multifocal intraocular1 report
- AcrySof® IQ PanOptix® Toric Trifocal IOL TFNT40Lens, multifocal intraocular1 report
- AcrySof® IQ PanOptix® Toric Trifocal IOL TFNT40Lens, multifocal intraocular1 report
- AcrySof® IQ PanOptix® Toric Trifocal IOL TFNT40Lens, multifocal intraocular1 report
- AcrySof® IQ PanOptix® Toric Trifocal IOL TFNT40Lens, multifocal intraocular1 report
- AcrySof® IQ PanOptix® Toric Trifocal IOL TFNT40Lens, multifocal intraocular1 report
- AcrySof® IQ PanOptix® Toric Trifocal IOL TFNT40Lens, multifocal intraocular1 report
Recent AcrySof IQ PanOptix Toric Trifocal IOL adverse event reports
The 15 most recent reports across all models, in the reporter's own words as published by the FDA.
InjurySep 11, 2026Adverse Event Without Identified Device or Use Problem
Patient problems: Insufficient Information
MAUDE report 50740896 ↗InjuryJun 1, 2026Adverse Event Without Identified Device or Use Problem
A NURSE REPORTED THAT AFTER SURGERY THE PATIENT EXPERIENCED THE SYMPTOM THAT APPEARS CLOUDY AFTER SURGERY IT BECAME MORE SEVERE AND THE EXCHANGE WAS CONDUCTED AND THE PATIENT ALSO EXPERIENCING WORSENING BLURRED VISION LEADING TO AN EXCHANGE BEING PERFORMED. THE INTRAOCULAR LENS (IOL) WAS SUBSEQUENTLY REMOVED AND REPLACED WITH UNSPECIFIED REPLACEMENT LENS DURING INITIAL IMPLANTATION PROCEDURE AND PROCEDURE WAS COMPLETED ON THE SAME DAY. ADDITIONAL INFORMATION HAS BEEN REQUESTED BUT IS NOT AVAILABLE AT THE TIME OF THIS REPORT.
Patient problems: Blurred Vision
MAUDE report 25348110 ↗InjuryMay 20, 2026Material Opacification; Material Deformation
A HEALTH CARE PROFESSIONAL REPORTED THAT AFTER AN INTRAOCULAR LENS (IOL) IMPLANT PROCEDURE, PATIENT COMPLAINING OF BLURRED VISION 6 YEARS POST CATARACT AND IOL IMPLANTATION. ADDITIONAL INFORMATION HAS BEEN RECEIVED AND STATED THAT PATIENT EXPERIENCED HAZY IOL, GLISTENINGS AND THE LENS WAS PLANNED TO BE EXPLANTED.
Patient problems: Blurred Vision
MAUDE report 25230719 ↗MalfunctionDec 31, 2025Material Deformation; Material Deformation
A HEALTHCARE PROFESSIONAL REPORTED THAT DURING A CATARACT SURGERY WITH INTRAOCULAR LENS (IOL) IMPLANT PROCEDURE, THE LENS HAD A SURFACE DEFECT. ADDITIONAL INFORMATION WAS RECEIVED BY STATING, THERE WAS NO PATIENT CONTACT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23934105 ↗MalfunctionDec 29, 2025Break; Break
A NON-HEALTH CARE PROFESSIONAL REPORTED THAT DURING INTRAOCULAR LENS (IOL) IMPLANTATION SURGERY THE LENS CAME OUT OF THE CARTRIDGE WITH ONE HAPTIC BROKEN. THE PHYSICIAN WAS UNABLE TO IMPLANT THE DAMAGED IOL WHICH HAD TO BE REMOVED INTO TWO PARTS. THE PATIENT WAS WAITING FOR ANOTHER LENS IMPLANTATION SURGERY.
Patient problems: Insufficient Information
MAUDE report 23908256 ↗MalfunctionOct 29, 2025Material Opacification; Material Deformation; Material Opacification; Material Deformation
A PHYSICIAN REPORTED THAT FOLLOWING AN INTRAOCULAR LENS (IOL) IMPLANT PROCEDURE, PATIENT EXPERIENCED GLISTENINGS AND FEELS LIKE HIS VISION WAS GETTING WORSE. THERE WAS SOME SORT OF HAZINESS OVER THE POSTERIOR ASPECT OF THE LENS. THE PATIENT HAD YAG (YTTRIUM ALUMINUM GARNET) PROCEDURE AND POSSIBLY VITRECTOMY FOR FLOATERS. ADDITIONAL INFORMATION WAS RECEIVED, IN THE SURGEON PROGNOSIS OVERALL OCULAR HEALTH WAS NORMAL. THE GLISTENINGS ON THE POSTERIOR SURFACE OF THE INTRAOCULAR LENS (IOL) SEEM TO BE LIMITING VISION. THERE ARE TWO MEDICAL DEVICE REPORTS ASSOCIATED WITH THIS PATIENT. THIS REPORT IS ASSOCIATED WITH THE RIGHT EYE.
Patient problems: Visual Impairment; Vitreous Floaters
MAUDE report 23413679 ↗InjurySep 2, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
ADDITIONAL INFORMATION WAS RECEIVED BY STATING, THE IOL WAS REPLACED WITH STANDARD MONOFOCAL NON-COMPANY LENS.
Patient problems: Blurred Vision
MAUDE report 22940094 ↗MalfunctionAug 21, 2025Break; Break
A NURSE REPORTED THAT DURING AN INTRAOCULAR LENS (IOL) IMPLANT PROCEDURE, DURING LOADING IT WAS NOTED THAT THE LENS HAPTIC WAS CUT OFF. THE PROCEDURE WAS COMPLETED WITH ANOTHER UNSPECIFIED LENS. THERE WAS NO PATIENT CONTACT OR HARM. ADDITIONAL INFORMATION HAS BEEN REQUESTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22861265 ↗MalfunctionJun 2, 2025Material Discolored; Material Deformation; Material Discolored; Material Deformation
A PHYSICIAN REPORTED THAT FOLLOWING AN INTRAOCULAR LENS (IOL) IMPLANT PROCEDURE, THE PATIENT WENT FOR CONSULTATION AND AFTER SLIT LAMP EXAMINATION, GLISTENING APPEARED ON LENS, HAD VISUAL ACUITY 8/10 TO 9/10 WITH A DECREASE IN VISION QUALITY. THE SURGEON DOES NOT WISH TO EXPLANT THE IMPLANT, AS THE SURGERY WAS PERFORMED TWO YEARS AGO (RISK OF CAPSULAR RUPTURE). ADDITIONAL INFORMATION HAS BEEN REQUESTED. THERE ARE TWO MEDICAL DEVICE REPORTS ASSOCIATED WITH THIS PATIENT. THIS FILE IS 1 OF 2.
Patient problems: Blurred Vision
MAUDE report 22124660 ↗MalfunctionJun 2, 2025Material Deformation; Material Deformation
A PHYSICIAN REPORTED THAT FOLLOWING AN INTRAOCULAR LENS (IOL) IMPLANT PROCEDURE, THE PATIENT WENT FOR CONSULTATION AND AFTER SLIT LAMP EXAMINATION, GLISTENING APPEARED ON LENS, HAD VISUAL ACUITY 8/10 TO 9/10 WITH A DECREASE IN VISION QUALITY. THE SURGEON DOES NOT WISH TO EXPLANT THE IMPLANT, AS THE SURGERY WAS PERFORMED TWO YEARS AGO (RISK OF CAPSULAR RUPTURE). ADDITIONAL INFORMATION HAS BEEN REQUESTED. THERE ARE TWO MEDICAL DEVICE REPORTS ASSOCIATED WITH THIS PATIENT. THIS FILE IS 2 OF 2.
Patient problems: Blurred Vision
MAUDE report 22123523 ↗InjuryApr 30, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
A NON-HEALTHCARE PROFESSIONAL REPORTED THAT FOLLOWING AN INTRAOCULAR LENS (IOL) IMPLANT PROCEDURE, THE PATIENT EXPERIENCED HYPEROPIC SHIFT. ADDITIONAL INFORMATION WAS RECEIVED AND STATED, THE LENS WAS NOT REPLACED BUT IN 2024 AUTUMN PATIENT GOT 1ST ADD ON PSEUDOPHAKIC LENS IN THE LEFT EYE. THE SURGEON EXPLAINED TO PATIENT THAT WHEN THEY COVER THE RIGHT EYE (UNOPERATED EYE) THE VISION WILL BE QUANTIFIABLY OKAY. THE RIGHT EYE WAS NOW NOT OPERATED; THE SURGERY WAS SCHEDULED FOR END OF (B)(6) 2025 FOR COMPANY LENS. THE SURGEON EXPECTS THAT IF BOTH EYES HAD DIFFRACTIVE TECHNOLOGY LENS, THE NEUROADAPTATION WOULD HELP THE PATIENT. SINCE IT LOOKS LIKE NOW THAT THE OD IS SOMEHOW DISTURBS THE PATIENT TO GET USED TO THE IOL. ADDITIONAL INFORMATION WAS RECEIVED AND STATED, ADD ON PSEUDOPHAKIC LENS WAS NOT AN COMPANY PRODUCT.
Patient problems: Visual Impairment
MAUDE report 21936568 ↗InjuryApr 30, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
A HEALTHCARE PROFESSIONAL REPORTED THAT, AFTER INTRAOCULAR LENS IMPLANTATION SURGERY, THE PATIENT EXPERIENCED CONTINUED DISCOMFORT. HENCE THE LENS WAS EXPLANTED AND REPLACED WITH ANOTHER LENS IN A SECONDARY PROCEDURE.
Patient problems: Visual Impairment
MAUDE report 21936313 ↗InjuryApr 17, 2025Material Opacification; Material Deformation; Material Opacification; Material Deformation
A PHYSICIAN REPORTED THAT FOLLOWING AN INTRAOCULAR LENS (IOL) IMPLANT PROCEDURE, PATIENT EXPERIENCED GLISTENINGS AND FEELS LIKE HIS VISION IS GETTING WORSE. THERE WAS SOME SORT OF HAZINESS OVER THE POSTERIOR ASPECT OF THE LENS. THE PATIENT HAD YAG (YTTRIUM ALUMINUM GARNET) PROCEDURE AND POSSIBLY VITRECTOMY FOR FLOATERS. ADDITIONAL INFORMATION HAS BEEN REQUESTED.
Patient problems: Visual Impairment; Vitreous Floaters
MAUDE report 21856298 ↗MalfunctionApr 2, 2025Scratched Material; Scratched Material
OTHER HEALTH CARE PROFESSIONAL REPORTED WITH A DESCRIPTION OF LENS HAD A MARK AFTER SURGERY. ADDITIONAL INFORMATION HAS BEEN REQUESTED.
Patient problems: Insufficient Information
MAUDE report 21750174 ↗MalfunctionMar 25, 2025Material Twisted/Bent; Material Twisted/Bent
A NURSE REPORTED THAT DURING AN INTRAOCULAR LENS (IOL) IMPLANT PROCEDURE, OPEN NOT USED LENS HAD A FAULTY HAPTIC ISSUE. ADDITIONAL INFORMATION WAS REQUESTED.
Patient problems: Insufficient Information
MAUDE report 21689938 ↗
Other Alcon Laboratories, Inc. products
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- CONSTELLATION HYPERVIT TOTAL PLUS5 models · 2,098 reports · 4 recalls
- Centurion5 models · 1,967 reports
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- MONARCH III2 models · 1,380 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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