FDA recall record

Custom Medical Specialties CMS-2193-R7 and CMS-1911-R3 Custom Biopsy Tray containing a BD recall — FDA Z-1234-2017

Sterility of syringe product could not be assured.

Class IIclassification
Z-1234-2017official record ID
Mar 1, 2017report date

Recall record at a glance

Official recordZ-1234-2017
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmCustom Medical Specialties, Inc.
Report dateMar 1, 2017
Recall initiation dateSep 20, 2016
Quantity80 syringes
LocationPine Level, NC, United States

Official product description

CMS-2193-R7 and CMS-1911-R3 Custom Biopsy Tray containing a BD 10cc LL Syringe, Sterile, Manufactured for CMS Custom Medical Specialties, Inc.

Why the product was recalled

Sterility of syringe product could not be assured.

Distribution information

US Distribution to ID and OR.

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: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.

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.

FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.

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