FDA recall record

ROi CPS Isolation Droplet Bundle Kit recall — FDA Z-2465-2020

Roi CPS, LLC has become aware of a labeling error that affects select custom procedure kits. The kits are labeled with an expiration date that is later…

Class IIclassification
Z-2465-2020official record ID
Jul 8, 2020report date

Recall record at a glance

Official recordZ-2465-2020
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmROi CPS LLC
Report dateJul 8, 2020
Recall initiation dateMay 19, 2020
Quantity24 kits
LocationRepublic, MO, United States

Official product description

Isolation Droplet Bundle Kit

Why the product was recalled

Roi CPS, LLC has become aware of a labeling error that affects select custom procedure kits. The kits are labeled with an expiration date that is later than that of the soonest kit component to expire in the kits.

Distribution information

Domestic distribution only to: MO and LA.

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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