Food, drugs, devices › Inmar Supply Chain Solutions, LLC
Food recall: Multiple FDA-regulated products. Pallets
Inmar Supply Chain Solutions, LLC (Arlington, TX) initiated this food recall on 15 Aug 2023; FDA lists 1 product record under event 92765, classified Class II.
FDA defines Class II as a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote. 53% of the 478 food enforcement events initiated in 2023 carry the same class.
Status: Terminated, terminated 1 Mar 2024. Initiation: voluntary: firm initiated. Inmar Supply Chain Solutions, LLC has 3 enforcement events on this register, with a median of 1 product record per event.
Recall classification reflects the relative degree of health hazard. Text in quotation marks is FDA's. openFDA export dated 28 Sep 2026.
Recalling firm
Inmar Supply Chain Solutions, LLC, Arlington, TX.
Reason for recall
"Potential exposure to rodents and rodent activity in the warehouse."
Distribution
"Nationwide"
Product records
| Recall number | Product | Quantity | Class | Status | Report date |
|---|---|---|---|---|---|
| F-1449-2023 | Multiple FDA-regulated products. Pallets | Unknown | Class II | Terminated | 30 Aug 2023 |
Context
Other enforcement events for Inmar Supply Chain Solutions, LLC
| Initiated | Product (first record) | Type | Class | Records |
|---|---|---|---|---|
| 24 Aug 2023 | Various Medical Products stored on pallets, including but not limited to bandages, tampons, condoms, blood glucose monit | Device | Class II | 1 |
| 14 Aug 2023 | All Over-The-Counter (OTC) drug products warehoused, salvaged, and sold by Inmar. | Drug | Class II | 1 |
All 3 events for Inmar Supply Chain Solutions, LLC
Questions and answers
Why was this food recalled?
FDA's record gives the reason for recall as: "Potential exposure to rodents and rodent activity in the warehouse."
What does Class II mean?
FDA classifies recalls by relative degree of health hazard. Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote.
Where was the product distributed?
FDA's distribution pattern field reads: "Nationwide"
Is the recall still ongoing?
FDA lists the status as Terminated; the termination date is 1 Mar 2024. "Terminated" means FDA has determined that all reasonable efforts to remove or correct the product have been made.
Where does this data come from?
openFDA enforcement reports (food, drug and device), CC0, export dated 28 Sep 2026. Text in quotation marks is FDA's. The FDA enforcement report linked above is authoritative.
Provenance
Source: openFDA food enforcement reports (CC0), export dated 28 Sep 2026; records grouped by FDA event number. The class shown for the event is the most severe class among its records. Errors in processing are corrected at the next build; see corrections.