Beekley Corporation

Complete recall history across all FDA and CPSC categories — 10 total recalls

Beekley Corporation appears in recall records across 1 category. This page consolidates all FDA food, drug, and medical device enforcement actions, plus CPSC consumer product recalls associated with this company. Recall data is sourced from openFDA and CPSC public databases.

Device Recalls (10)

FDA medical device enforcement actions by Beekley Corporation

Date Product Reason Class
Jun 13, 2018 O-SPOT REF 791, 791S Adhere to skin for marking and identifying moles in ... There is a potential for imaging artifact to mimic calcifications on patient'... Class II
Jun 13, 2018 TomoSPOT REF 782, 782S, 783, 783S, 784, 784S, 785 & 785S Adhere to skin f... There is a potential for imaging artifact to mimic calcifications on patient'... Class II
Jun 13, 2018 S-SPOT REF 777, 777S Adhere to skin for marking and identifying moles in ... There is a potential for imaging artifact to mimic calcifications on patient'... Class II
May 8, 2017 Beekley Medical 0-SPOT Mammography Skin Markers REF 652 Mammography Skin Marker 0 -SPOT (REF 652) product was mis-labeled with A-SPOT... Class III
Jun 19, 2013 Beekley Spots Light Image O-Spots for Mammography Catalog Number: 252 Pro... Light Image O-Spots Dispenser mislabeled as Soft n' Stretchy Light Image S-Spots Class III
Jul 9, 2012 Beekley O-Spots Floral Skin Markers -Order Number: 752 Product Usage: Mam... Digital Skin Mammography Marker separating from the backing of the spot mate... Class II
Jul 9, 2012 Beekley A-Spots Floral Skin Markers -Order Number: 751 Product Usage: Mam... Digital Skin Mammography Marker separating from the backing of the spot mate... Class II
Jul 9, 2012 Beekley S-Spots Floral Skin Markers -Order Number: 750 Product Usage: Mam... Digital Skin Mammography Marker separating from the backing of the spot mate... Class II
Jul 9, 2012 Beekley Altus Floral Skin Markers -Order Number: 754 Product Usage: desig... Digital Skin Mammography Marker separating from the backing of the spot mate... Class II
Jul 2, 2012 Bella Blanket Protective Coverlet, for Mammography, 18cm x 25cm or 24cm x 30c... Imaging artifact can occur on mammogram result Class II

Frequently Asked Questions

A high number of recalls does not necessarily indicate that a company is unsafe. Large manufacturers that produce thousands of products across multiple categories will statistically appear in recall databases more frequently. What matters more is the severity of each recall (Class I being the most serious), the speed of response, and whether the company proactively identified and addressed the issue. Companies with robust safety programs often catch problems earlier.

Food, drug, and medical device recall data comes from the FDA's openFDA enforcement database, which contains all FDA enforcement reports. Consumer product recall data comes from the U.S. Consumer Product Safety Commission (CPSC). Both sources are public government databases that are updated regularly. RecallCheck aggregates these sources to provide a unified view of a company's recall history.

The FDA classifies recalls into three categories. Class I is the most serious — there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. Class II means the product may cause temporary or medically reversible health problems, or the probability of serious consequences is remote. Class III is the least serious — the product is unlikely to cause adverse health consequences. CPSC product recalls do not use this classification system.

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