FDA Medical Device Recalls (openFDA)
Beekley Corporation: TomoSPOT REF 782, 782S, 783, 783S, 784, 784S, 785 & 785S Adhere to skin for marking and identifying moles in mammography.
- Recall number
- Z-2832-2018
- Recalling firm
- Beekley Corporation
- Product
- TomoSPOT REF 782, 782S, 783, 783S, 784, 784S, 785 & 785S Adhere to skin for marking and identifying moles in mammography.
- Status
- Terminated
- Initiated
- 2018-06-13
- Posted
- not on file
- Terminated
- 2018-11-13
- Reason
- There is a potential for imaging artifact to mimic calcifications on patient's mammograms
- Root cause
- Nonconforming Material/Component
- Action
- On June 14, 2018, Beekley Medical issued an "URGENT MEDICAL DEVICE RECALL" notice dated June 13, 2018 to customers. The notice described the products, problem and actions to be taken. Customers are advised to do the following: - Inspect stock and quarantine affected product - complete and return the acknowledgement response form via fax to: 1-800-735-1234 or mail. - contact firm if inventory of affected product remains with customers at 1-800-233-5539 between 8:00am - 5:30pm EDT. If you have any issues occurred or for further question, contact Quality Assurance & Regulatory Manager at 1-800-233-5539x434.
- Quantity
- 3,384,024 pieces in total.
- Distribution
- Worldwide Distribution: US (Nationwide) and countries of; AUSTRALIA, AUSTRIA, BAHRAIN, CANADA, GREAT BRITAIN, ISRAEL, SAUDI ARABIA, SOUTH AFRICA & UNITED ARAB EMIRATES.
- Lot, serial or model codes
- REF 782 - Lot Numbers: 05311801 05211801 02221801 04181802 03051801 03071802 04181804 05081801 03131801 02121801 03301802 05141801 03141801 05101801 03271801 05161801 02161801 03021802 04111801 05011801 05171802 02211801 04051802 04271801 04251801 05161802 03141802 05181801 04121801 05221802 04161802 04171801 04181803 05301802 04241802 05011802 02271802 02271803 02071802 02261802 02261803 05291803 REF 782S - Lot Numbers: 02221801 03271801 04121801 REF 783 - Lot Numbers: 04131801 03071801 02281801 03121801 05151801 04101801 05041801 03021801 05181803 02081801 03261801 05221801 02061801 04181801 04201801 05071801 03161801 04061801 05181802 04231802 03091802 03171801 REF 783S - Lot Numbers: 02221801 04021801 REF 784 - Lot Numbers: 05231801 03061801 02261801 03211801 02141801 03211802 05091801 04261802 REF 784S - Lot Numbers: 02221801 04021801 04121801 REF 785 Lot Numbers: 05111801 04191801 REF 785S Lot Numbers: 04021801 04121801
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- JAC
- Firm FEI
- 3000204334
- Firm city
- Bristol
- Firm state
- CT
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28