Food, drugs, devices › Inmar Supply Chain Solutions, LLC
Drug recall: All Over-The-Counter (OTC) drug products warehoused, salvaged, and sold by Inmar.
Inmar Supply Chain Solutions, LLC (Arlington, TX) initiated this drug recall on 14 Aug 2023; FDA lists 1 product record under event 92884, 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. 59% of the 281 drug enforcement events initiated in 2023 carry the same class.
Status: Ongoing. Initiation: n/a. 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
"CGMP Deviations: Potential exposure to rodents and rodent activity in the distribution center. Also, due to unusually hot weather, FDA Recalled Products may have been subjected to temperatures in excess of storage condition instructions on product labeling."
Distribution
"Separate Distribution List (salvage buyers) provided by Inmar and will be uploaded. Final customer distribution unknown."
Product records
| Recall number | Product | Quantity | Class | Status | Report date |
|---|---|---|---|---|---|
| D-1104-2023 | All Over-The-Counter (OTC) drug products warehoused, salvaged, and sold by Inmar. | Unknown | Class II | Ongoing | 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 |
| 15 Aug 2023 | Multiple FDA-regulated products. Pallets | Food | Class II | 1 |
All 3 events for Inmar Supply Chain Solutions, LLC
Questions and answers
Why was this drug recalled?
FDA's record gives the reason for recall as: "CGMP Deviations: Potential exposure to rodents and rodent activity in the distribution center. Also, due to unusually hot weather, FDA Recalled Products may have been subjected to temperatures in excess of storage condition instructions on product labeling."
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: "Separate Distribution List (salvage buyers) provided by Inmar and will be uploaded. Final customer distribution unknown."
Is the recall still ongoing?
FDA lists the status as Ongoing. "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 drug 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.