DENTEMP ONE STEP .077OZ, SKU 902139
Reported: November 15, 2023 Initiated: October 4, 2023 #Z-0265-2024
Product Description
DENTEMP ONE STEP .077OZ, SKU 902139
Reason for Recall
Products were stored outside of labeled temperature requirements.
Details
- Recalling Firm
- Family Dollar Stores, Llc.
- Units Affected
- 329,044 total units
- Distribution
- Distributed to Family Dollar stores in the following states: GA, AL, MS, FL, LA, AR, AZ, KS, TX, OK, CO, NM, NE, UT, NV, WY, ID, SD, ND, CA, MT, OR, WA.
- Location
- Chesapeake, VA
Frequently Asked Questions
What product was recalled? ▼
DENTEMP ONE STEP .077OZ, SKU 902139. Recalled by Family Dollar Stores, Llc.. Units affected: 329,044 total units.
Why was this product recalled? ▼
Products were stored outside of labeled temperature requirements.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on November 15, 2023. Severity: Moderate. Recall number: Z-0265-2024.
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