FDA recall record

Stradis Medical, LLC dba Stradis Healthcare HENRY SCHEIN, RHINO PACK, Item No.570-3070 recall — FDA Z-0528-2023

Medical and surgical procedure trays and kits underwent certain manufacturing conditions that may result in the outer bag being incompletely sealed, which…

Class IIclassification
Z-0528-2023official record ID
Dec 21, 2022report date

Recall record at a glance

Official recordZ-0528-2023
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmStradis Medical, LLC dba Stradis Healthcare
Report dateDec 21, 2022
Recall initiation dateNov 2, 2022
Quantity328 units
LocationPeachtree Corners, GA, United States

Official product description

HENRY SCHEIN, RHINO PACK, Item No.570-3070

Why the product was recalled

Medical and surgical procedure trays and kits underwent certain manufacturing conditions that may result in the outer bag being incompletely sealed, which may result in a breach in the sterility of the kit.

Distribution information

US nationwide distribution, and Canada.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: E-Mail.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

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