SchickRecalls & reported problems across all models

We found 16 models of Schick by Dentsply International Inc. in the FDA's device registry (GUDID). Together they are named in 72 adverse event reports in the FDA's MAUDE database, received between Feb 10, 2026 and Jul 7, 2026 — classified as 72 malfunctions.

The most frequently reported specific device problem is “Poor Quality Image” (69 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

Most reported Schick problems

Schick models

16 models, most reported first. Each model has its own page with its reports, recalls and device details.

• Schick 100008633

  Solid state x-ray imager (flat panel/digital imager)
  18 reports
• Schick 100008625

  Solid state x-ray imager (flat panel/digital imager)
  9 reports
• Schick 100008624

  Solid state x-ray imager (flat panel/digital imager)
  8 reports
• Schick 100008634

  Solid state x-ray imager (flat panel/digital imager)
  7 reports
• Schick 100008286

  Solid state x-ray imager (flat panel/digital imager)
  5 reports
• Schick 100008651

  Solid state x-ray imager (flat panel/digital imager)
  4 reports
• Schick B1218000

  Unit, x-ray, intraoral
  4 reports
• Schick B1218001

  Solid state x-ray imager (flat panel/digital imager)
  4 reports
• Schick 100008628

  Solid state x-ray imager (flat panel/digital imager)
  3 reports
• Schick B1218051

  Solid state x-ray imager (flat panel/digital imager)
  3 reports
• Schick 100008720

  Unit, x-ray, intraoral
  2 reports
• Schick 100007219

  Solid state x-ray imager (flat panel/digital imager)
  1 report
• Schick 100008290

  Unit, x-ray, intraoral
  1 report
• Schick 100008640

  Solid state x-ray imager (flat panel/digital imager)
  1 report
• Schick 100008652

  Unit, x-ray, intraoral
  1 report
• Schick B1209120

  Solid state x-ray imager (flat panel/digital imager)
  1 report

Recent Schick adverse event reports

The 15 most recent reports across all models, in the reporter's own words as published by the FDA.

• MalfunctionJul 7, 2026Failure to Transmit Record; Communication or Transmission Problem

  WHILE THE CUSTOMER WAS USING A SCHICK33 S2 SENSOR/3.0 CABLE RMA KIT 9', THEY ALLEGE EXPERIENCING IMAGE TRANSMISSION ISSUES WHEN AN X-RAY IMAGE WAS TAKEN AND AN ADDITIONAL IMAGE WAS REQUIRED. NO INJURY WAS REPORTED FROM THE ALLEGED EVENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 25730769 ↗
• MalfunctionMay 27, 2026Failure to Read Input Signal; Communication or Transmission Problem

  WHILE THE CUSTOMER WAS USING A PART OF AN INTRAORAL SENSOR SYSTEM, THEY ALLEGE THERE WAS AN X-RAY IMAGE TRANSMISSION ISSUE WHERE THE X-RAY IMAGE WAS NOT CAPTURED AFTER RADIATION HAS OCCURRED (TRANSMISSION FAILURE). NO INJURY WAS REPORTED FROM THE ALLEGED EVENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 25300028 ↗
• MalfunctionMay 27, 2026Poor Quality Image

  WHILE THE CUSTOMER WAS USING A PART OF AN INTRAORAL SENSOR SYSTEM, THEY ALLEGE EXPERIENCING IMAGE QUALITY ISSUES WHEN AN X-RAY IMAGE WAS TAKEN AND AN ADDITIONAL IMAGE WAS REQUIRED. NO INJURY WAS REPORTED FROM THE ALLEGED EVENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 25299414 ↗
• MalfunctionMay 6, 2026Intermittent Communication Failure

  WHILE THE CUSTOMER WAS USING A PART OF AN INTRAORAL SENSOR SYSTEM, THEY ALLEGE EXPERIENCING CONNECTIVITY ISSUES WHEN AN X-RAY IMAGE WAS TAKEN OR AN ADDITIONAL IMAGE WAS REQUIRED. NO INJURY WAS REPORTED FROM THE ALLEGED EVENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 25092775 ↗
• MalfunctionApr 17, 2026Poor Quality Image

  WHILE THE CUSTOMER WAS USING A PART OF AN INTRAORAL SENSOR SYSTEM, SCHICK33 S2 SENSOR SHIP KIT, 6FT THEY ALLEGE EXPERIENCING IMAGE QUALITY ISSUES WHEN AN X-RAY IMAGE WAS TAKEN AND AN ADDITIONAL IMAGE WAS REQUIRED. NO INJURY WAS REPORTED FROM THE ALLEGED EVENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24912814 ↗
• MalfunctionMar 31, 2026Poor Quality Image

  WHILE THE CUSTOMER WAS USING A PART OF AN INTRAORAL SENSOR SYSTEM, SCHICK33 S2 SENSOR SHIP KIT, 6FT, THEY ALLEGE THERE WAS A DEVICE RESPONSE ISSUE WHERE THE X-RAY IMAGE WAS NOT CAPTURED AFTER RADIATION HAS OCCURRED (NO DEVICE OUTPUT). NO INJURY WAS REPORTED FROM THE ALLEGED EVENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24744223 ↗
• MalfunctionMar 30, 2026Poor Quality Image

  WHILE THE CUSTOMER WAS USING A PART OF AN INTRAORAL SENSOR SYSTEM, SCHICK33 S2 STARTER KIT/3.0 INTERFACE 6', THEY ALLEGE EXPERIENCING CONNECTIVITY ISSUES WHEN AN X-RAY IMAGE WAS TAKEN OR AN ADDITIONAL IMAGE WAS REQUIRED. NO INJURY WAS REPORTED FROM THE ALLEGED EVENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24730136 ↗
• MalfunctionMar 23, 2026Poor Quality Image

  WHILE THE CUSTOMER WAS USING A PART OF AN INTRAORAL SENSOR SYSTEM, SCHICK33 S2 SENSOR SHIP KIT/3.0 CABLE 9', THEY ALLEGE EXPERIENCING IMAGE QUALITY ISSUES WHEN AN X-RAY IMAGE WAS TAKEN AND AN ADDITIONAL IMAGE WAS REQUIRED. NO INJURY WAS REPORTED FROM THE ALLEGED EVENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24661995 ↗
• MalfunctionMar 23, 2026Poor Quality Image

  WHILE THE CUSTOMER WAS USING A PART OF AN INTRAORAL SENSOR SYSTEM, SCHICK AE USB INTERFACE, THEY ALLEGE EXPERIENCING IMAGE QUALITY ISSUES WHEN AN X-RAY IMAGE WAS TAKEN AND AN ADDITIONAL IMAGE WAS REQUIRED. NO INJURY WAS REPORTED FROM THE ALLEGED EVENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24661698 ↗
• MalfunctionMar 23, 2026Poor Quality Image

  WHILE THE CUSTOMER WAS USING A PART OF AN INTRAORAL SENSOR SYSTEM, SCHICK33 S2 SENSOR SHIP KIT/3.0 CABLE 9', THEY ALLEGE THERE WAS AN X-RAY IMAGE TRANSMISSION ISSUE WHERE THE X-RAY IMAGE WAS NOT CAPTURED AFTER RADIATION HAS OCCURRED (TRANSMISSION FAILURE). NO INJURY WAS REPORTED FROM THE ALLEGED EVENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24660970 ↗
• MalfunctionMar 23, 2026Poor Quality Image

  WHILE THE CUSTOMER WAS USING A PART OF AN INTRAORAL SENSOR SYSTEM, THEY ALLEGE THERE WAS AN X-RAY IMAGE TRANSMISSION ISSUE WHERE THE X-RAY IMAGE WAS NOT CAPTURED AFTER RADIATION HAS OCCURRED (TRANSMISSION FAILURE). NO INJURY WAS REPORTED FROM THE ALLEGED EVENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24660951 ↗
• MalfunctionMar 23, 2026Poor Quality Image

  WHILE THE CUSTOMER WAS USING A PART OF AN INTRAORAL SENSOR SYSTEM, THEY ALLEGE EXPERIENCING CONNECTIVITY ISSUES WHEN AN X-RAY IMAGE WAS TAKEN OR AN ADDITIONAL IMAGE WAS REQUIRED. NO INJURY WAS REPORTED FROM THE ALLEGED EVENT. THIS EVENT REQUIRES MEDICAL INTERVENTION TO RETAKE THE X-RAY IMAGE. THIS ALSO EXPOSES THE PATIENT TO ADDITIONAL RADIATION DUE TO THE NEED TO RETAKE THE X-RAY IMAGE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24660936 ↗
• MalfunctionMar 23, 2026Poor Quality Image

  WHILE THE CUSTOMER WAS USING A PART OF AN INTRAORAL SENSOR SYSTEM, SCHICK33 S2 SENSOR SHIP KIT, 9FT, THEY ALLEGE THERE WAS AN X-RAY IMAGE TRANSMISSION ISSUE WHERE THE X-RAY IMAGE WAS NOT CAPTURED AFTER RADIATION HAS OCCURRED (TRANSMISSION FAILURE). NO INJURY WAS REPORTED FROM THE ALLEGED EVENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24660913 ↗
• MalfunctionMar 16, 2026Poor Quality Image

  WHILE THE CUSTOMER WAS USING A PART OF AN INTRAORAL SENSOR SYSTEM, THEY ALLEGE EXPERIENCING CONNECTIVITY ISSUES WHEN AN X-RAY IMAGE WAS TAKEN OR AN ADDITIONAL IMAGE WAS REQUIRED. NO INJURY WAS REPORTED FROM THE ALLEGED EVENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24607452 ↗
• MalfunctionMar 16, 2026Poor Quality Image

  WHILE THE CUSTOMER WAS USING A PART OF AN INTRAORAL SENSOR SYSTEM, THEY ALLEGE EXPERIENCING IMAGE QUALITY ISSUES WHEN AN X-RAY IMAGE WAS TAKEN AND AN ADDITIONAL IMAGE WAS REQUIRED. NO INJURY WAS REPORTED FROM THE ALLEGED EVENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24607407 ↗

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