Device recalls

Access Testosterone assay, Catalog Number 33560

Beckman Coulter, Inc. · Inadequate preventative maintenance (PM) performed on the scales of the RPL5 fill line, led to splashing (cross-contamination) between the wells of testosteron…

Open, ClassifiedEquipment maintenanceZ-1901-2025
Open FDA's page for this record
Cfres ID
213728
Product res number
Z-1901-2025
Event date initiated
2025-05-05
Event date posted
2025-06-02
Recall status
Open, Classified
Res event number
96824
Product code
CDZ
Product description
Access Testosterone assay, Catalog Number 33560
Code info
UDI-DI: 15099590231347; Serial Number: 538081
Firm FEI number
2122870
Recalling firm
Beckman Coulter, Inc.
Address 1
1000 Lake Hazeltine Dr
City
Chaska
State
MN
Postal code
55318-1037
Additional info contact
Ian Pilcher 952-448-4848
Root cause description
Equipment maintenance
Product quantity
70 units
Distribution pattern
US State: FL. UAE, Vietnam
Reason for recall

Inadequate preventative maintenance (PM) performed on the scales of the RPL5 fill line, led to splashing (cross-contamination) between the wells of testosterone reagent packs lot 538081, which could potentially result in up to a 34% increase or a 23% decrease in patient results.

Action

An URGENT MEDICAL DEVICE RECALL notification letter dated 4/23/25 was sent to customers. ACTION: Discontinue using and discard all remaining Access Testosterone reagent packs from the lot listed above. Beckman Coulter recommends performing a retrospective review on patient results generated with the Access Testosterone lot listed above and assessing the need for retesting. Contact your local Beckman Coulter representative for replacement product requests. Beckman Coulter is no longer distributing the affected Access Testosterone reagent pack lot number and has corrected the manufacturing issue that led to cross-contamination. Please share this information with your laboratory staff and retain this notification as part of your laboratory Quality System documentation. If you have forwarded any of the affected product listed above to another laboratory, please provide them a copy of this letter. So that we are assured you have received this important communication, please respond within 10 days in one of the following ways: Electronically, if you received this communication via email. Manually, complete and return the enclosed Response Form. If you have any questions regarding this notice, please contact our Customer Support Center: From our website: http://www.beckmancoulter.com If you need replacement product: o Complete the attached Replacement Order Form and email to askbeckman@beckman.com or fax to (866) 294-7850 OR o Call Client Services at (800) 526-3821

K numbers
K223405
Harmonized identifiers (openFDA)
Device name
Radioimmunoassay, Testosterones And Dihydrotestosterone
Medical specialty description
Clinical Chemistry
Regulation number
862.1680
Device class
1
K number
K093421, K182521, K840187, K014120, K971823, K023091, K152155, K151529, K955440, K811536, K791999, K191533, K844423, K802661, K001086, K102814, K181017, K860130, K083867, K233480, K915823, K021326, K191350, K152185, K780792, K854674, K862483, K934562, K041866, K800776, K120009, K223405, K854671, K032881, K802135, K801666, K151986, K000043, K122793, K983212 +49 more
Registration number
2032682, 1036362, 3003030793, 3007349751, 3002642396, 9610746, 2432235, 2250051, 2032087, 3003559191, 1219913, 2182595, 3002806944, 1319681, 9612316, 3004192065, 1222302, 2122870, 8010132, 2419955, 3006198300, 8023018, 8020888, 3010324880, 3002809144, 3007361513, 3012963943, 3022178699, 3005529799, 3005984081, 3000308930, 2133982, 3007111389, 1415939, 3005333358, 8031673, 9615037, 1832216, 3007118747, 2018685 +16 more
FEI number
3004185580, 1036362, 3002807272, 3003030793, 3002485711, 3007349751, 3002642396, 3003261083, 2432235, 2250051, 3003559191, 1219913, 2182595, 3002806944, 3004192065, 3000717645, 2967, 2122870, 3002676602, 3006198300, 2419955, 1000306617, 1000121039, 3002806559, 3003952975, 3010324880, 3002809144, 3007361513, 3003355251, 3002806808, 3012963943, 1000136573, 3022178699, 3005529799, 3005984081, 3000308930, 3007111389, 1415939, 3005333358, 1832216 +16 more
Wholesale access for licensed clinicians.

Free to join: your NPI is checked against the federal registry at signup, then wholesale pricing and the professional shelves open.

Data from openFDA, FDA's public API. FDA says not to rely on it to make decisions about medical care and to treat every result as unvalidated; confirm against FDA's own record and the product labeling. Not medical or legal advice.