Beekley Corporation: FDA recalls
FDA enforcement reports name Beekley Corporation as the recalling firm in 5 events. The events have 10 product records. The recalls started from 2012 to 2018. All the events are device recalls.
It is important to note that most of the time recall classifications are determined after the recalling firm provides all of the information needed to determine the risk posed to public health. The classification and posting in the FDA Enforcement Report should not be seen as an expansion or change to a firm’s voluntary public warning.
FDA publishes these words. Source: FDA, Enforcement Reports, Important Note, read on . openFDA export of .
Enforcement events
5 events, newest first.
| Initiated | Product (first record) | Type | Class | Records | Status |
|---|---|---|---|---|---|
| 13 Jun 2018 | O-SPOT REF 791, 791S Adhere to skin for marking and identifying moles in mammography. | Device | Class II | 3 | Terminated |
| 8 May 2017 | Beekley Medical 0-SPOT Mammography Skin Markers REF 652 | Device | Class III | 1 | Terminated |
| 19 Jun 2013 | Beekley Spots Light Image O-Spots for Mammography Catalog Number: 252 Product Usage: To identify raised moles in Mammography | Device | Class III | 1 | Terminated |
| 9 Jul 2012 | Beekley S-Spots Floral Skin Markers -Order Number: 750 Product Usage: Mammography Skin Markers for marking: moles, scars, palpable masses or areas of concern | Device | Class II | 4 | Terminated |
| 2 Jul 2012 | Bella Blanket Protective Coverlet, for Mammography, 18cm x 25cm or 24cm x 30cm, Product Code: 311. The purpose of the product is to remove the cold by placing this sheet between the patient’s breast and the imaging receptor plate. | Device | Class II | 1 | Terminated |
An event with 1 product record and a class that is not Class I has no page. It has a row in this table.
Enforcement event: All the product records that have one FDA event number. This site shows one event on one page.
Recalling firm: The firm that the FDA record names for a recall.
Follow by RSS:Food, drug and device recallsFDA Class I recalls
Type and class
| Type | Events |
|---|---|
| Device | 5 |
| Class | Events |
|---|---|
| Class II | 3 |
| Class III | 2 |
- Share of the events of the firm in Class I
- 0%
- Share of all events on the register in Class I
- 18%
- Events with the status Ongoing
- 0
openFDA, about the status: FDA does not update the status of a recall after the recall has been classified according to its level of hazard. As such, the status of a recall (open, completed, or terminated) will remain unchanged after published in the Enforcement Reports.
Source: openFDA, Drug Recall Enforcement Reports, Disclaimer.
Events by year
Official channels
- FDA enforcement reportsThe FDA search of the weekly enforcement reports.
- FDA: recalls, market withdrawals and safety alertsThe recall notices on the FDA site.
- FDA: report a problemThe FDA page that shows where a report about a product goes.
- FDA MedWatchThe FDA safety reporting program for drugs and medical devices.
Cite this page
Recall Register. Beekley Corporation: FDA recalls. https://recallregister.com/firm/beekley-corporation/. Source: openFDA enforcement reports. Data through .
Sources
- Source
- openFDA enforcement reports
- Licence
- CC0 1.0
- Export date
- 28 Sep 2026
- State of the firm address
- CT
The firm name is the spelling in the FDA records. A company with 2 spellings has 2 pages.
A firm with more products can have more recalls. This site does not compare one firm with a different firm. How the register is made. Report an error.
Questions
- Which classes do the FDA recalls of Beekley Corporation have?
- Class II: 3 events. Class III: 2 events. The class is for the product of a recall. It is not a class of the firm.
- What is the newest FDA recall of Beekley Corporation?
- FDA event 80558, which the firm started on 13 Jun 2018. The first product in the record is:
O-SPOT REF 791, 791S Adhere to skin for marking and identifying moles in mammography.
- How many FDA recalls of Beekley Corporation have the status Ongoing?
- No event has the status Ongoing in the openFDA file. openFDA says about the status:
FDA does not update the status of a recall after the recall has been classified according to its level of hazard. As such, the status of a recall (open, completed, or terminated) will remain unchanged after published in the Enforcement Reports.