Sensicare Green Surgical Glove — Class II medical device recall Z-0162-2018
Terminated recall by Medline Industries Inc, reported 2017-11-29, distributed in AK, AL, AR, AZ, CA, CO, CT, DC…. Possible open seal on top portion of the package. Could cause breach of sterility.
| Recall number | Z-0162-2018 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Medline Industries Inc, Northfield, IL, United States |
| Recall initiated | 2017-10-23 |
| Classified | 2017-11-21 |
| Reported by FDA | 2017-11-29 |
| Terminated | 2021-04-06 |
| Distributed | AK, AL, AR, AZ, CA, CO, CT, DC, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, NE, NJ, NM, NV, NY, OH, OK, OR, PA, PR, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV, WY |
| Countries outside the US | CA |
| Quantity | 8,000 units |
| Reason classes | sterility, packaging |
| Lot numbers | 701893369485 |
| Model numbers | MSG1285 |
Product
Sensicare Green Surgical Glove, PI, LF, PF. Packaged in a poly/poly peel pouch with Sunoco films, sterile. Surgical glove.
Reason for recall
Possible open seal on top portion of the package. Could cause breach of sterility.
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-0162-2018. 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.