3M Ranger — Class II medical device recall Z-2632-2017
Terminated recall by 3M Company - Health Care Business, reported 2017-07-05, distributed in TX. It was discovered that one Ranger Pressure lnfusor Model 145, SN: 100873, produced a left chamber pressure tha
| Recall number | Z-2632-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | 3M Company - Health Care Business, Saint Paul, MN, United States |
| Recall initiated | 2017-05-22 |
| Classified | 2017-06-26 |
| Reported by FDA | 2017-07-05 |
| Terminated | 2018-06-14 |
| Distributed | TX |
| Quantity | 1 units |
| Serial numbers | 100873 |
| Model numbers | 145 |
Product
3M Ranger(TM) Pressure Infusor, Model 145, SKU 70200792979 The 3M Ranger Pressure Infusor is a hardware device intended to provide pressure to I.V. solution bags when rapid infusion of liquids is required.
Reason for recall
It was discovered that one Ranger Pressure lnfusor Model 145, SN: 100873, produced a left chamber pressure that was slightly below the manufacturing specification.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2632-2017. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.