FDA Device recall Z-2096-2013
OLA Buffer For Laboratory Use
- FDA Device
- Class III
- terminated
- Published 2013-09-04
On 2013-09-04 the FDA classified a Class III recall of OLA Buffer For Laboratory Use by Celera, citing the package insert for FG OLA Buffer, GPR displayed the wrong concentration of ¿M instead of the correct mM unit.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2096-2013 |
| Classification | Class III |
| Status | terminated |
| Initiated | 2013-07-12 |
| Published | 2013-09-04 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Celera |
| Distribution | US |
Product
OLA Buffer For Laboratory Use; Contents: 1 tube with buffered solution containing MgCl2 (80 ¿M) and KCL (300 ¿M. 10.0ml.) PN: 50003300; Store at d - 15¿C. Product Usage: General Purpose Reagent for laboratory use.
Reason
The package insert for FG OLA Buffer, GPR displayed the wrong concentration of ¿M instead of the correct mM unit.
Identifiers
| code_info | Lot numbers: 10016853, 10017390, 10020343, 10021820 and 10022594. Expiry dates 12/5/2010, 06/15/2012, 09/08,2012, 08/13/2013 and 02/21/2014. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2096-2013%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.