Persona The Personalized KneeRecalls & reported problems across all models
Zimmer, Inc. · 77 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1,396
- Deaths reported
- 0
- Injuries reported
- 29
- Recalls
- 0
We found 77 models of Persona The Personalized Knee by Zimmer, Inc. in the FDA's device registry (GUDID). Together they are named in 1,396 adverse event reports in the FDA's MAUDE database, received between Oct 10, 2019 and Aug 18, 2026 — classified as 29 injuries, 1,367 malfunctions.
The most frequently reported specific device problem is “Fracture” (1,106 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 Persona The Personalized Knee problems
Device problems
- Fracture1,106
- Detachment of Device or Device Component253
- Adverse Event Without Identified Device or Use Problem17
- Naturally Worn15
- Mechanical Jam6
- Positioning Failure5
- Device Markings/Labelling Problem3
- Difficult to Insert3
Patient problems
- No Clinical Signs, Symptoms or Conditions1,227
- No Patient Involvement84
- No Known Impact Or Consequence To Patient43
- No Consequences Or Impact To Patient24
- Pain12
- Ambulation or Postural Difficulties4
- Swelling/ Edema4
- Thrombosis/Thrombus4
Persona The Personalized Knee models
77 models, most reported first. Each model has its own page with its reports, recalls and device details.
- Persona® The Personalized Knee® 42-5270-005-05PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER234 reports
- Persona® The Personalized Knee® 42-5170-005-05PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER185 reports
- Persona® The Personalized Knee® 42-5170-003-03PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER135 reports
- Persona® The Personalized Knee® 42-5270-007-07PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER129 reports
- Persona® The Personalized Knee® 42-5170-007-07PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER116 reports
- Persona® The Personalized Knee® 42-5270-003-03PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER112 reports
- Persona® The Personalized Knee® 42-5279-003-00PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER31 reports
- Persona® The Personalized Knee® 42-5399-018-31Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + additive/metal/polymer + additive28 reports
- Persona® The Personalized Knee® 42-5279-005-00PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER24 reports
- Persona® The Personalized Knee® 42-5279-005-02PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER24 reports
- Persona® The Personalized Knee® 42-5279-003-02PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER23 reports
- Persona® The Personalized Knee® 42-5279-007-01PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER21 reports
- Persona® The Personalized Knee® 42-5279-007-03PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER18 reports
- Persona® The Personalized Knee® 42-5174-005-10PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER16 reports
- Persona® The Personalized Knee® 42-5279-003-01PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER16 reports
- Persona® The Personalized Knee® 42-5279-007-00PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER16 reports
- Persona® The Personalized Knee® 42-5274-005-10PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER15 reports
- Persona® The Personalized Knee® 42-5279-005-03PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER15 reports
- Persona® The Personalized Knee® 42-5279-005-04PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER15 reports
- Persona® The Personalized Knee® 42-5270-005-10PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER13 reports
- Persona® The Personalized Knee® 42-5279-005-01PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER12 reports
- Persona® The Personalized Knee® 42-5176-005-05Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + additive/metal/polymer + additive11 reports
- Persona® The Personalized Knee® 42-5176-007-07PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER11 reports
- Persona® The Personalized Knee® 42-5279-003-03PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER11 reports
- Persona® The Personalized Knee® 42-5279-003-04PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER10 reports
- Persona® The Personalized Knee® 42-5279-007-02PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER10 reports
- Persona® The Personalized Knee® 42-5099-040-20PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER10 reports
- Persona® The Personalized Knee® 42-5279-007-04PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER9 reports
- Persona® The Personalized Knee® 42-5274-007-10PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER8 reports
- Persona® The Personalized Knee® 42-5270-006-10PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER7 reports
- Persona® The Personalized Knee® 42-5170-004-10PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER6 reports
- Persona® The Personalized Knee® 42-5170-005-10PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER6 reports
- Persona® The Personalized Knee® 42-5174-007-10PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER6 reports
- Persona® The Personalized Knee® 42-5360-075-02PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, COATED, POLYMER/METAL/POLYMER6 reports
- Persona® The Personalized Knee® 42-5274-004-10PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER5 reports
- Persona® The Personalized Knee® 42-5360-079-02PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER5 reports
- Persona® The Personalized Knee® 42-5174-004-10PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER4 reports
- Persona® The Personalized Knee® 42-5176-003-03PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, COATED, POLYMER/METAL/POLYMER4 reports
- Persona® The Personalized Knee® 42-5276-005-05Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + additive/metal/polymer + additive4 reports
- Persona® The Personalized Knee® 42-5276-007-07Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + additive/metal/polymer + additive4 reports
- Persona® The Personalized Knee® 42-5360-067-01Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + additive/metal/polymer + additive4 reports
- Persona® The Personalized Knee® 42-5360-067-02Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + additive/metal/polymer + additive4 reports
- Persona® The Personalized Knee® 42-5170-006-10PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER3 reports
- Persona® The Personalized Knee® 42-5174-008-10PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER3 reports
- Persona® The Personalized Knee® 42-5360-064-02PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER3 reports
- Persona® The Personalized Knee® 42-5399-022-25Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + additive/metal/polymer + additive3 reports
- Persona® The Personalized Knee® 42-5399-022-27PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, COATED, POLYMER/METAL/POLYMER3 reports
- Persona® The Personalized Knee® 42-5170-005-15PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER2 reports
- Persona® The Personalized Knee® 42-5174-009-10PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER2 reports
- Persona® The Personalized Knee® 42-5174-010-10PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER2 reports
- Persona® The Personalized Knee® 42-5176-005-10PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER2 reports
- Persona® The Personalized Knee® 42-5274-010-10PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER2 reports
- Persona® The Personalized Knee® 42-5360-071-01PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, COATED, POLYMER/METAL/POLYMER2 reports
- Persona® The Personalized Knee® 42-5360-075-01Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + additive/metal/polymer + additive2 reports
- Persona® The Personalized Knee® 42-5870-007-21Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + additive/metal/polymer + additive2 reports
- Persona® The Personalized Knee® 42-5170-001-01PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 report
- Persona® The Personalized Knee® 42-5170-003-13PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 report
- Persona® The Personalized Knee® 42-5170-007-17PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 report
- Persona® The Personalized Knee® 42-5170-009-09PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 report
- Persona® The Personalized Knee® 42-5172-005-10PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 report
- Persona® The Personalized Knee® 42-5174-006-10PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 report
- Persona® The Personalized Knee® 42-5176-007-10Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + additive/metal/polymer + additive1 report
- Persona® The Personalized Knee® 42-5176-010-10PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, COATED, POLYMER/METAL/POLYMER1 report
- Persona® The Personalized Knee® 42-5270-001-01PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 report
- Persona® The Personalized Knee® 42-5270-004-10PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 report
- Persona® The Personalized Knee® 42-5270-005-15PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 report
- Persona® The Personalized Knee® 42-5270-007-17PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 report
- Persona® The Personalized Knee® 42-5272-005-10PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 report
- Persona® The Personalized Knee® 42-5272-006-10PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 report
- Persona® The Personalized Knee® 42-5274-008-10PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 report
- Persona® The Personalized Knee® 42-5276-003-03Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + additive/metal/polymer + additive1 report
- Persona® The Personalized Knee® 42-5276-004-10PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, COATED, POLYMER/METAL/POLYMER1 report
- Persona® The Personalized Knee® 42-5276-005-10Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + additive/metal/polymer + additive1 report
- Persona® The Personalized Knee® 42-5276-005-15PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, COATED, POLYMER/METAL/POLYMER1 report
- Persona® The Personalized Knee® 42-5276-008-10Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + additive/metal/polymer + additive1 report
- Persona® The Personalized Knee® 42-5360-079-01PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 report
- Persona® The Personalized Knee® 42-5360-083-01PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 report
Recent Persona The Personalized Knee adverse event reports
The 15 most recent reports across all models, in the reporter's own words as published by the FDA.
MalfunctionAug 18, 2026Detachment of Device or Device Component
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50300236 ↗MalfunctionAug 17, 2026Component Missing
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50288333 ↗MalfunctionAug 12, 2026Detachment of Device or Device Component
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50226591 ↗InjuryAug 5, 2026Adverse Event Without Identified Device or Use Problem
It was reported that the patient has experienced moderate to severe pain and difficulty with activities approximately one (1) year following a right knee arthroplasty. Patient was recommended to modify activities and shoe wear and to pursue physical therapy, deep tissue massage and weight loss.Attempts have been made, however, no additional information is available.
Patient problems: Ambulation or Postural Difficulties; Pain
MAUDE report 50148105 ↗MalfunctionJul 30, 2026Fracture
It was reported that peg drill fractured at the distal extremity. The surgical technique was utilized. No pieces fell inside the patient. There was no surgical delay. Attempts have been made and all available information has been provided.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50088415 ↗MalfunctionJul 28, 2026Detachment of Device or Device Component
It was reported that a disassembled shim was returned. There was no patient involvement. Attempts have been made and no further information has been provided.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50063551 ↗MalfunctionJul 28, 2026Detachment of Device or Device Component
It was reported that a disassembled shim was returned. There was no patient involvement. Attempts have been made and no further information has been provided.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50063485 ↗InjuryJul 28, 2026Unstable; Loosening of Implant Not Related to Bone-Ingrowth
It was reported that the patient is tentatively awaiting a left knee arthroplasty revision to address tibial component loosening, pain, swelling and instability after a fall.Initial operative notes noted no intraoperative complications.Attempts have been made and no further information has been provided.
Patient problems: Aseptic loosening; Joint Laxity; Osteolysis; Pain; Radiolucent Lines; Swelling/ Edema
MAUDE report 50053723 ↗MalfunctionJul 22, 2026Fracture
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25906838 ↗MalfunctionJul 20, 2026Fracture
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25874884 ↗MalfunctionJun 29, 2026Detachment of Device or Device Component
IT WAS REPORTED THAT SHIM WAS MISSING BEARINGS. THE ISSUE WAS DISCOVERED DURING A ROUTINE QUALITY INSPECTION. ALL PIECES HAVE NOT RETURNED. ATTEMPTS HAVE BEEN MADE AND ALL AVAILABLE INFORMATION HAS BEEN PROVIDED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25654102 ↗MalfunctionJun 29, 2026Detachment of Device or Device Component
IT WAS REPORTED THAT SHIM WAS MISSING BEARINGS. THE ISSUE WAS DISCOVERED DURING A ROUTINE QUALITY INSPECTION. ALL PIECES HAVE NOT RETURNED. ATTEMPTS HAVE BEEN MADE AND ALL AVAILABLE INFORMATION HAS BEEN PROVIDED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25654088 ↗MalfunctionJun 29, 2026Detachment of Device or Device Component
IT WAS REPORTED THAT SHIM WAS MISSING BEARINGS. THE ISSUE WAS DISCOVERED DURING A ROUTINE QUALITY INSPECTION. ALL PIECES HAVE NOT RETURNED. ATTEMPTS HAVE BEEN MADE AND ALL AVAILABLE INFORMATION HAS BEEN PROVIDED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25654069 ↗MalfunctionJun 29, 2026Detachment of Device or Device Component
IT WAS REPORTED THAT SHIM WAS MISSING BEARINGS. THE ISSUE WAS DISCOVERED DURING A ROUTINE QUALITY INSPECTION. ALL PIECES HAVE NOT RETURNED. ATTEMPTS HAVE BEEN MADE AND ALL AVAILABLE INFORMATION HAS BEEN PROVIDED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25654068 ↗MalfunctionJun 17, 2026Fracture
IT WAS REPORTED THAT THE TIP OF A DRILL BROKE OFF. THE SURGICAL TECHNIQUE WAS UTILIZED, THERE WAS NO SURGICAL DELAY, THERE WERE NO FOREIGN BODIES RETAINED. ATTEMPTS HAVE BEEN MADE AND NO FURTHER INFORMATION HAS BEEN PROVIDED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25535817 ↗
Other Zimmer, Inc. products
- PERSONA364 models · 2,000 reports · 3 recalls
- PERSONA Vivacit-E285 models · 1,152 reports
- NexGen198 models · 842 reports · 4 recalls
- Affixus18 models · 1 reports · 17 recalls
- PERSONA Natural Tibia25 models · 417 reports · 2 recalls
- NexGen Legacy119 models · 319 reports · 3 recalls
- Alliance32 models · 275 reports · 2 recalls
- Comprehensive18 models · 103 reports · 3 recalls
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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