FIRST RESPONSE 2 CT, SKU 902343
Reported: August 24, 2022 Initiated: June 23, 2022 #Z-1537-2022
Product Description
FIRST RESPONSE 2 CT, SKU 902343
Reason for Recall
Affected product was not appropriately stored in temperature-controlled areas between April 30, 2022 - June 10, 2022.
Details
- Recalling Firm
- Family Dollar Stores, Llc.
- Units Affected
- 77
- Distribution
- Product distributed to Family Dollar retail stores in US nationwide.
- Location
- Chesapeake, VA
Frequently Asked Questions
What product was recalled? ▼
FIRST RESPONSE 2 CT, SKU 902343. Recalled by Family Dollar Stores, Llc.. Units affected: 77.
Why was this product recalled? ▼
Affected product was not appropriately stored in temperature-controlled areas between April 30, 2022 - June 10, 2022.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on August 24, 2022. Severity: Moderate. Recall number: Z-1537-2022.
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