FDA recall record

MEVION S250 Radiation therapy system recall — FDA Z-0767-2016

The treatment table positioning belt can slip gear positions, resulting in deviation of patient setup and treatment positions from the time of slippage…

Class IIclassification
Z-0767-2016official record ID
Feb 17, 2016report date

Recall record at a glance

Official recordZ-0767-2016
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmMevion Medical Systems, Inc.
Report dateFeb 17, 2016
Recall initiation dateNov 18, 2015
Quantity4
LocationLittleton, MA, United States

Official product description

MEVION S250 Radiation therapy system

Why the product was recalled

The treatment table positioning belt can slip gear positions, resulting in deviation of patient setup and treatment positions from the time of slippage until the discovery of slippage and the halting of treatment.

Distribution information

US nationwide distribution including FL, NJ, OK, and MO.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

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MEVION S250i, MEVION S250 recall — FDA Z-2406-2020

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