Persona Trabecular MetalRecalls & reported problems across all models
Zimmer, Inc. · 57 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
1 open recall names at least one Persona Trabecular Metal model. Check whether yours is affected in the recall details, and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 198
- Deaths reported
- 0
- Injuries reported
- 182
- Recalls
- 1
We found 57 models of Persona Trabecular Metal by Zimmer, Inc. in the FDA's device registry (GUDID). Together they are named in 198 adverse event reports in the FDA's MAUDE database, received between Sep 30, 2019 and Sep 29, 2026 — classified as 182 injuries, 16 malfunctions.
The most frequently reported specific device problem is “Unstable” (17 reports).
1 FDA recall record name at least one of these models by its device identifier, 1 still open.
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
Persona Trabecular Metal recalls
FDA recall records that name at least one of these models by its device identifier, newest first. Each recall usually covers specific models or lots, so check the details.
- May 11, 2026Open, Classified
Firm received a complaint with no clinical impact in which a posterior augment was found within the distal augment package.
Z-2578-2026 · Root cause: Labeling Change Control · Recall details · FDA record ↗
Most reported Persona Trabecular Metal problems
Device problems
- Adverse Event Without Identified Device or Use Problem136
- Unstable17
- Loosening of Implant Not Related to Bone-Ingrowth16
- Insufficient Device Problem Information9
- Malposition of Device5
- Packaging Problem5
- Device Damaged Prior to Receipt by User4
- Patient Device Interaction Problem3
Patient problems
- Pain102
- Loss of Range of Motion40
- Swelling/ Edema36
- Failure of Implant21
- Joint Laxity20
- Scar Tissue19
- No Clinical Signs, Symptoms or Conditions18
- Fall12
Persona Trabecular Metal models
57 models, most reported first. Each model has its own page with its reports, recalls and device details.
- Persona® Trabecular Metal® 42-5572-066-10PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 recall0 reports
- Persona® Trabecular Metal® 42-5028-070-02PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER12 reports
- Persona® Trabecular Metal® 42-5450-005-12PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, COATED, POLYMER/METAL/POLYMER11 reports
- Persona® Trabecular Metal® 42-5028-062-02Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + additive/metal/polymer + additive10 reports
- Persona® Trabecular Metal® 42-5450-005-10PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER10 reports
- Persona® Trabecular Metal® 42-5028-064-02PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER9 reports
- Persona® Trabecular Metal® 42-5450-010-11PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, COATED, POLYMER/METAL/POLYMER9 reports
- Persona® Trabecular Metal® 42-5028-068-01Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + additive/metal/polymer + additive8 reports
- Persona® Trabecular Metal® 42-5028-064-01PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, COATED, POLYMER/METAL/POLYMER6 reports
- Persona® Trabecular Metal® 42-5028-066-01Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + additive/metal/polymer + additive6 reports
- Persona® Trabecular Metal® 42-5028-066-02Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + additive/metal/polymer + additive6 reports
- Persona® Trabecular Metal® 42-5022-064-02PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER6 reports
- Persona® Trabecular Metal® 42-5450-005-11PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, COATED, POLYMER/METAL/POLYMER6 reports
- Persona® Trabecular Metal® 42-5028-060-02PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER5 reports
- Persona® Trabecular Metal® 42-5022-062-01PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, COATED, POLYMER/METAL/POLYMER5 reports
- Persona® Trabecular Metal® 42-5450-005-08PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER5 reports
- Persona® Trabecular Metal® 42-5450-010-12PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER5 reports
- Persona® Trabecular Metal® 42-5028-070-01PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, COATED, POLYMER/METAL/POLYMER4 reports
- Persona® Trabecular Metal® 42-5028-074-02Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + additive/metal/polymer + additive4 reports
- Persona® Trabecular Metal® 42-5022-062-02PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, COATED, POLYMER/METAL/POLYMER4 reports
- Persona® Trabecular Metal® 42-5022-064-01Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + additive/metal/polymer + additive4 reports
- Persona® Trabecular Metal® 42-5022-066-02PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER4 reports
- Persona® Trabecular Metal® 42-5022-068-02Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + additive/metal/polymer + additive4 reports
- Persona® Trabecular Metal® 42-5028-062-01Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + additive/metal/polymer + additive3 reports
- Persona® Trabecular Metal® 42-5028-074-01PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, COATED, POLYMER/METAL/POLYMER3 reports
- Persona® Trabecular Metal® 42-5022-060-01PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER3 reports
- Persona® Trabecular Metal® 42-5022-066-01PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER3 reports
- Persona® Trabecular Metal® 42-5022-068-01PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, COATED, POLYMER/METAL/POLYMER3 reports
- Persona® Trabecular Metal® 42-5450-005-13PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER3 reports
- Persona® Trabecular Metal® 42-5450-010-13PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, COATED, POLYMER/METAL/POLYMER3 reports
- Persona® Trabecular Metal® 42-5028-058-01PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, COATED, POLYMER/METAL/POLYMER2 reports
- Persona® Trabecular Metal® 42-5028-058-02PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER2 reports
- Persona® Trabecular Metal® 42-5028-060-01Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + additive/metal/polymer + additive2 reports
- Persona® Trabecular Metal® 42-5028-068-02Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + additive/metal/polymer + additive2 reports
- Persona® Trabecular Metal® 42-5008-058-02Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + additive/metal/polymer + additive2 reports
- Persona® Trabecular Metal® 42-5022-058-02Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + additive/metal/polymer + additive2 reports
- Persona® Trabecular Metal® 42-5022-070-02PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, COATED, POLYMER/METAL/POLYMER2 reports
- PERSONA™ Trabecular Metal™ 42-5002-060-02PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 report
- Persona® Trabecular Metal® 42-5002-058-01PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 report
- Persona® Trabecular Metal® 42-5002-060-02Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + additive/metal/polymer + additive1 report
- Persona® Trabecular Metal® 42-5002-064-01Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + additive/metal/polymer + additive1 report
- Persona® Trabecular Metal® 42-5002-066-02Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + additive/metal/polymer + additive1 report
- Persona® Trabecular Metal® 42-5008-058-01PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, COATED, POLYMER/METAL/POLYMER1 report
- Persona® Trabecular Metal® 42-5008-064-02PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 report
- Persona® Trabecular Metal® 42-5008-066-01PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 report
- Persona® Trabecular Metal® 42-5008-068-01Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + additive/metal/polymer + additive1 report
- Persona® Trabecular Metal® 42-5008-068-02Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + additive/metal/polymer + additive1 report
- Persona® Trabecular Metal® 42-5008-070-02PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, COATED, POLYMER/METAL/POLYMER1 report
- Persona® Trabecular Metal® 42-5022-056-02PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 report
- Persona® Trabecular Metal® 42-5022-058-01PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, COATED, POLYMER/METAL/POLYMER1 report
- Persona® Trabecular Metal® 42-5022-070-01Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + additive/metal/polymer + additive1 report
- Persona® Trabecular Metal® 42-5028-054-01PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 report
- Persona® Trabecular Metal® 42-5028-056-01PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, COATED, POLYMER/METAL/POLYMER1 report
- Persona® Trabecular Metal® 42-5028-056-02PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, COATED, POLYMER/METAL/POLYMER1 report
- Persona® Trabecular Metal® 42-5450-015-23PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, COATED, POLYMER/METAL/POLYMER1 report
- Persona® Trabecular Metal® 42-5450-010-14PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, COATED, POLYMER/METAL/POLYMER1 report
- Persona® Trabecular Metal® 42-5572-054-10PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 report
Recent Persona Trabecular Metal adverse event reports
The 15 most recent reports across all models, in the reporter's own words as published by the FDA.
InjurySep 29, 2026Adverse Event Without Identified Device or Use Problem
Patient problems: Joint Laxity; Pain
MAUDE report 50934070 ↗MalfunctionAug 24, 2026Packaging Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50411756 ↗InjuryJul 31, 2026Adverse Event Without Identified Device or Use Problem
It was reported that the patient underwent a knee arthroplasty revision to address tibial tray migration resulting in instability. Upon removal of the components, femoral osteolysis around the metaphyseal region of the femur was identified that extended to the posterior condyles both medially and laterally. All components were revised and replaced.Attempts have been made, however, no additional information is available.
Patient problems: Joint Laxity; Osteolysis
MAUDE report 50100380 ↗InjuryJul 14, 2026Loosening of Implant Not Related to Bone-Ingrowth
IT WAS REPORTED THAT A PATIENT IS BEING CONSIDERED FOR A DFR TO ARCOS STEM CONVERSION. THE PATIENT PREVIOUSLY HAD ZSS COMPONENTS IMPLANTED, HOWEVER THE PATIENT¿S BONE QUALITY IS NOT SUFFICIENT FOR CEMENT FIXATION. THE PATIENT ORIGINALLY HAD A ZSS CEMENTED STEM IMPLANTED, IT BECAME LOOSE AND THEN ANOTHER ZSS CEMENTED STEM WAS RE-IMPLANTED, AND NOW THE CURRENT INDWELLING CEMENTED STEM IS ALSO LOOSENING. THE SURGEON IS REQUESTING A CUSTOM ZSS TO ARCOS ADAPTER TO MATE WITH THE CURRENT INDWELLING ZSS FEMUR TO REPLACE THE CURRENT INDWELLING CEMENTED ZSS STEM WITH A SPLINED ARCOS STEM. SURGEON DOES NOT WANT TO REVISE THE WELL-FIXED TIBIAL IMPLANTS AND IS JUST REQUESTING A CUSTOM ZSS TO ARCOS ADAPTER TO MATE WITH THE ZSS FEMORAL COMPONENT AND AN ARCOS STEM. THE TIBIAL CONE FROM THE CURRENT INDWELLING IS IMPLANTED ON THE FEMORAL SIDE THROUGH THE FEMORAL STEM, THEREFORE, THE TIBIAL COMPONENTS ON THE TIBIAL SIDE ARE NOT GOING TO BE REPLACED, BUT THE ONE ON THE FEMORAL SIDE WILL BE REMOVED. IT IS THOUGHT THAT THE SURGEON IMPLANTED IT ON THE FEMORAL SIDE TO TRY AND AID IN GETTING THE STEM TO REMAIN FIXED. THE TARGETED REVISION DATE IS EARLY NOVEMBER. ATTEMPTS TO OBTAIN ADDITIONAL INFORMATION HA
Patient problems: Aseptic loosening; Pain
MAUDE report 25813709 ↗MalfunctionMay 19, 2026Packaging Problem
IT WAS REPORTED THAT THE PACKAGING OF A FEMORAL COMPONENT APPEARED HEAT AFFECTED AND HAD SHRUNK AROUND THE FEMORAL COMPONENT. THE SHRUNKEN PACKAGING MAY COMPROMISE STERILITY OF IMPLANT. NO FURTHER INFORMATION IS AVAILABLE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25218751 ↗InjuryApr 30, 2026Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED A PATIENT UNDERWENT RIGHT KNEE A TWO-STAGE REVISION FOR INFECTION. APPROXIMATELY SEVEN MONTHS LATER THE PATIENT BEGAN TO HAVE INTERMITTENT PAIN AND SWELLING. TWO YEARS AND FIVE MONTHS LATER THE PATIENT REPORTED AN INCREASE IN PAIN AND WAS PRESCRIBED PHYSICAL THERAPY. ALL IMPLANTS REMAIN IN PLACE.
Patient problems: Pain; Swelling/ Edema
MAUDE report 25045531 ↗InjuryApr 30, 2026Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED A PATIENT UNDERWENT RIGHT KNEE A TWO-STAGE REVISION FOR INFECTION. APPROXIMATELY SEVEN MONTHS LATER THE PATIENT BEGAN TO HAVE INTERMITTENT PAIN AND SWELLING. TWO YEARS AND FIVE MONTHS LATER THE PATIENT REPORTED AN INCREASE IN PAIN AND WAS PRESCRIBED PHYSICAL THERAPY. ALL IMPLANTS REMAIN IN PLACE.
Patient problems: Pain; Swelling/ Edema
MAUDE report 25045517 ↗MalfunctionApr 9, 2026Device Damaged Prior to Receipt by User
IT WAS REPORTED THE IMPLANT PACKAGING APPEARED TO BE DAMAGED PRIOR TO USE. THE DEVICE WAS NOT USED AND NO PATIENT IMPACT AND NO ADVERSE EVENTS HAVE BEEN REPORTED AS A RESULT OF THE MALFUNCTION. ALL AVAILABLE INFORMATION HAS BEEN PROVIDED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24835076 ↗InjuryMar 16, 2026Adverse Event Without Identified Device or Use Problem
NO FURTHER EVENT INFORMATION IS AVAILABLE AT THE TIME OF THIS REPORT.
Patient problems: Loss of Range of Motion
MAUDE report 24613404 ↗MalfunctionFeb 10, 2026Device Damaged Prior to Receipt by User
IT WAS REPORTED THAT UPON OPENING THE PACKAGING OF THE FEMORAL DISTAL AUGMENTATION, THE SURGEON DISCOVERED A HOLE IN THE INNER BAG, SO HE COMPLETED THE OPERATION USING A NEW ONE. ATTEMPTS TO OBTAIN ADDITIONAL INFORMATION HAVE BEEN MADE; HOWEVER, NO MORE INFORMATION IS AVAILABLE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24303679 ↗InjuryFeb 9, 2026Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT THE PATIENT UNDERWENT A RIGHT KNEE ARTHROPLASTY REVISION TO ADDRESS INSTABILITY APPROXIMATELY ONE (1) MONTH POST-OPERATIVELY. ATTEMPTS HAVE BEEN MADE, HOWEVER, NO ADDITIONAL INFORMATION IS AVAILABLE.
Patient problems: Joint Laxity
MAUDE report 24293746 ↗InjuryFeb 2, 2026Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT THE PATIENT UNDERWENT AN INITIAL LEFT KNEE SURGERY. APPROXIMATELY 3.5 YEARS POSTOP, THE PATIENT WAS REVISED DUE TO PAIN. ATTEMPTS HAVE BEEN MADE AND ALL AVAILABLE INFORMATION HAS BEEN PROVIDED.
Patient problems: Pain
MAUDE report 24232897 ↗MalfunctionJan 26, 2026Packaging Problem
IT WAS REPORTED THE IMPLANT PACKAGING APPEARED TO BE MELTED PRIOR TO USE. THE DEVICE WAS NOT USED AND A SECONDARY IMPLANT WAS RETRIEVED TO COMPLETE THE PROCEDURE. THERE WAS NO PATIENT IMPACT AND NO ADVERSE EVENTS HAVE BEEN REPORTED AS A RESULT OF THE MALFUNCTION. ALL AVAILABLE INFORMATION HAS BEEN PROVIDED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24182919 ↗InjuryJan 13, 2026Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT THE PATIENT UNDERWENT AN INITIAL LEFT TOTAL KNEE ARTHROPLASTY. APPROXIMATELY 3.5 YEARS POST-OP, THE PATIENT WAS EXPERIENCING PAIN WITHOUT RELIEF FROM PHYSIOTHERAPY, A PAIN MANAGEMENT SPECIALIST, AND REHABILITATION. IMAGING REVEALED INCREASED UPTAKE AT THE PATELLA AND MEDIAL TIBIAL AREA. SUBSEQUENTLY, THE PATIENT WAS REVISED. ALL COMPONENTS WERE REVISED. THERE WAS NO LOOSENING SEEN, HOWEVER, THE SURGEON NOTED AREAS OF SOFTER BONE. ATTEMPTS HAVE BEEN MADE AND ALL AVAILABLE INFORMATION HAS BEEN PROVIDED.
Patient problems: Pain
MAUDE report 24052775 ↗InjuryJan 7, 2026Adverse Event Without Identified Device or Use Problem
NO FURTHER INFORMATION IS AVAILABLE AT THE TIME OF THIS REPORT.
Patient problems: Joint Laxity; Pain
MAUDE report 23988209 ↗
Other Zimmer, Inc. products
- PERSONA364 models · 2,000 reports · 3 recalls
- Persona The Personalized Knee77 models · 1,396 reports
- 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
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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