Probe Cover — Class II medical device recall Z-1911-2021
Terminated recall by Exact Medical Manufacturing, Inc., reported 2021-06-30, distributed in FL, GA, MT, NY, OH, PR. No 510k for the product to be used in a natural or surgical opening to the body
| Recall number | Z-1911-2021 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Exact Medical Manufacturing, Inc., Lancaster, NY, United States |
| Recall initiated | 2021-04-29 |
| Classified | 2021-06-21 |
| Reported by FDA | 2021-06-30 |
| Terminated | 2022-05-26 |
| Distributed | FL, GA, MT, NY, OH, PR |
| Quantity | 12,650 units |
| Lot numbers | 2003E242, 2003E829, 2004E033, 2005E164, 2005E165, 2005E176, 2005E440, 2011E107, 2011E250, 2012E509, 2101E070 |
| Model numbers | A-AU-0980N |
Product
Probe Cover, 6"x96" poly, tapered end, w 3 bands-Ultrasonic Transducer Cover Item ID: A-AU-0980N
Reason for recall
No 510k for the product to be used in a natural or surgical opening to the body
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-1911-2021. 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.