CLASS II ONGOING Device recall · Reported 4 Oct 2023 · FDA Enforcement Report
Various Medical Products stored on pallets recalled
Inmar Supply Chain Solutions is recalling Various Medical Products stored on pallets, including but not limited to bandages, distributed nationwide in the US. The recall was initiated on 24 Aug 2023 and the FDA has classified it as Class II.
Check your package
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
Recall details
- Recall number
- Z-2634-2023
- FDA event ID
- 92933
- Recalling firm
- Inmar Supply Chain Solutions, Arlington, TX
- Classification
- Class II
- Status
- Ongoing
- Recall initiated
- 24 Aug 2023
- FDA classified
- 25 Sep 2023
- Reported
- 4 Oct 2023
- Type
- Voluntary: Firm initiated
- Customers notified by
- Press Release
- Reason category
- Foreign Material
- Device type
- Insulin Pumps & Glucose Monitors
Timeline
| 24 Aug 2023 | Recall initiated by company | |
| 25 Sep 2023 | Classified by FDA | +32 days |
| 4 Oct 2023 | Published in enforcement report | +9 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Various medical devices potentially exposed to rodent and rodent activity. In addition, medical devices may have been subjected to temperatures in excess of storage requirements on product labeling.
Foreign material recalls cover pieces of metal, plastic, glass, wood or other objects that got into the product during processing and could cause injury if eaten.
Product as listed by the FDA
Various Medical Products stored on pallets, including but not limited to bandages, tampons, condoms, blood glucose monitors, adult diapers, COVID-19 test kits, and pregnancy tests.
Where it was distributed
US Nationwide distribution.
Questions about this recall
Is Various Medical Products stored on pallets, including but not limited to bandages recalled?
Yes. Inmar Supply Chain Solutions recalled Various Medical Products stored on pallets, including but not limited to bandages on 24 Aug 2023. The recall is Class II and its status is Ongoing. Recall number Z-2634-2023.
Why was it recalled?
Various medical devices potentially exposed to rodent and rodent activity. In addition, medical devices may have been subjected to temperatures in excess of storage requirements on product labeling.
Which lots are affected?
Various
Where was it sold?
US Nationwide distribution.
What should I do if I have it?
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
More recalls from Inmar Supply Chain Solutions
All 3| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS II | All Over-The-Counter recalled by Inmar Supply Chain Solutions | Inmar Supply Chain Solutions | Foreign Material | TX |
| Food | CLASS II | Multiple FDA-regulated products recalled by Inmar Supply Chain Solutions | Inmar Supply Chain Solutions | Foreign Material | Nationwide |
Other Insulin Pumps & Glucose Monitors recalls
All 459| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | MiniMed Insulin Pump recalled by Medtronic MiniMed | Medtronic MiniMed | Other | Nationwide |
| Device | CLASS II | MiniMed Insulin Pump recalled by Medtronic MiniMed | Medtronic MiniMed | Other | Nationwide |
| Device | CLASS II | MiniMed Insulin Pump recalled by Medtronic MiniMed | Medtronic MiniMed | Other | Nationwide |
| Device | CLASS II | MiniMed Insulin Pump recalled by Medtronic MiniMed | Medtronic MiniMed | Lead & Heavy Metals | Nationwide |
| Device | CLASS I | Omnipod (Eros) Pod recalled by Insulet | Insulet | Lead & Heavy Metals | Nationwide |