PerkinElmer 226 Sample Collection Device
Reported: June 10, 2020 Initiated: December 19, 2017 #Z-2264-2020
Product Description
PerkinElmer 226 Sample Collection Device
Reason for Recall
PerkinElmer 226 Sample Collection Devices Lot Number 40020001 had serial numbers printed on the pack labels that did not match the serial number range of the devices contained within the pack.
Details
- Recalling Firm
- PerkinElmer Health Sciences, Inc.
- Units Affected
- 164,952 devices
- Distribution
- US distribution in the state of Ohio
- Location
- Greenville, SC
Frequently Asked Questions
What product was recalled? ▼
PerkinElmer 226 Sample Collection Device. Recalled by PerkinElmer Health Sciences, Inc.. Units affected: 164,952 devices.
Why was this product recalled? ▼
PerkinElmer 226 Sample Collection Devices Lot Number 40020001 had serial numbers printed on the pack labels that did not match the serial number range of the devices contained within the pack.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on June 10, 2020. Severity: Low. Recall number: Z-2264-2020.
Related Recalls
FDA Devices Moderate
Convenience Kits 1. 25GA Convenience Kit - FNX VS0644.25-FNX 2. 25GA Convenience Kit - FXX VS0644.25-FXX 3.2…
Vortex Surgical Inc. · 2026-02-11
FDA Devices Moderate
COULTER DxH Diluent, REF 628017 COULTER DxH ECO Diluent REF C67250 For use as an isotonic buffered diluent in conju…
Beckman Coulter, Inc. · 2026-02-11
FDA Devices Moderate
Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number: KD-V411M-1520 Product Description: These inst…
Olympus Corporation of the Americas · 2026-02-11
FDA Devices Moderate
Product Name: Disposable Triple Lumen Sphincterotome Model/Catalog Number: KD-401Q-0330 Product Description: These in…
Olympus Corporation of the Americas · 2026-02-11
FDA Devices Moderate
Product Name: Lumipulse pTau 217 Plasma Controls Model/Catalog Number: 81558 Software Version: Not Applicable Produc…
Fujirebio Diagnostics, Inc. · 2026-02-11