RapidSorb 851.008.01SRecalls & reported problems
Synthes GmbH · 1.5MM RAPID RESORBABLE ADAPTION PLATE 8 HOLES-STERILE · Class 2 · Implant
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10887587063607), received between Feb 22, 2023 and Feb 22, 2023 — classified as 1 injury.
3 other recalls cover devices cleared under the same FDA submission (K030069, K062789); they may or may not involve this specific model.
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. How this data works · Data updated Oct 13, 2026.
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem1
Patient problems
- Inflammation1
- Swelling/ Edema1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryFeb 22, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
DEVICE REPORT FROM JAPAN REPORTS AN EVENT AS FOLLOWS: IT WAS REPORTED THAT THIS WAS AN ORIF SURGERY TREATING ZYGOMATIC FRACTURE PERFORMED ON (B)(6) 2021, WITH THE PRODUCTS IN QUESTION. THE SURGERY WAS COMPLETED SUCCESSFULLY WITH NO SURGICAL DELAY. FROM ABOUT 3 MONTHS AFTER SURGERY, SWELLING AND DISAPPEARANCE OF THE CHEEK ON THE AFFECTED SIDE HAVE BEEN REPEATED. AT FIRST, THE SURGEON THOUGHT THE SYMPTOM WAS A FOREIGN BODY REACTION CAUSED BY AN ABSORBABLE PLATE AND DECIDED TO CONTINUE TO FOLLOW UP UNTIL THE PLATE WAS ABSORBED. HOWEVER, THE SYMPTOM HAS BEEN PERSISTING 1 YEAR AND 5 MONTHS AFTER THE SURGERY. THE SURGEON COMMENTED THAT THE CLINICAL SYMPTOM WAS SUSPECTED TO BE ANGIOEDEMA (QUINCKE'S EDEMA). NO FURTHER INFORMATION IS AVAILABLE. THIS REPORT IS FOR A 1.5MM RAPID RESORBABLE ADAPTION PLATE 8 HOLES-STERILE. THIS IS REPORT 1 OF 3 FOR (B)(4).
Patient problems: Inflammation; Swelling/ Edema
MAUDE report 16419029 ↗
Recalls under the same FDA submission
These recalls involve devices cleared under K030069, K062789. One submission often covers many models, so check the product and lot details in each record.
- Z-1920-2016 · May 2, 2016 · Terminated1.5 mm Rapid Resorb Orbt1 F1 P1 w/Bending Template / 35 mm - Sterile, Rapid Resorbable Fixation System. 1.5 mm Rapid Resorbable Orbital Floor Plate with Bending Template. Intend
- Z-1919-2016 · May 2, 2016 · Terminated1.5 mm Rapid Resorb Orbt1 F1 P1 w/Bending Template / 30 mm - Sterile, Rapid Resorbable Fixation System. 1.5 mm Rapid Resorbable Orbital Floor Plate with Bending Template. Intend
- Z-1918-2016 · May 2, 2016 · Terminated1.5 mm Rapid Resorb Orbt1 F1 P1 w/Bending Template / 24 mm - Sterile, Rapid Resorbable Fixation System. 1.5 mm Rapid Resorbable Orbital Floor Plate with Bending Template. Inte
Other PLATE, BONE devices
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- RapidSorb 806.004.02SSynthes GmbH · PLATE, BONE146 reports
- TruMatch SD980.001Materialise NV · Plate, Bone1 recall21 reports
- Matrix 04.511.225.01Synthes GmbH · PLATE, BONE62 reports
- NA 400.834Synthes GmbH · PLATE, BONE58 reports
- TruMatch SD980.016Materialise NV · Plate, Bone55 reports
- ProPlan CMF SD900.101Materialise NV · Plate, Bone1 recall1 report
- TruMatch SD980.013Materialise NV · Plate, Bone1 recall0 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.