FDA recall record

QURA S.R.L Spectrum Medical Quantum Standard heat exchanger recall — FDA Z-2277-2021

Product labeled as sterile may not have been adequately sterilized. In addition, these devices were imported to the US distributor, but the devices are…

Class IIclassification
Z-2277-2021official record ID
Aug 18, 2021report date

Recall record at a glance

Official recordZ-2277-2021
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmQURA S.R.L.
Report dateAug 18, 2021
Recall initiation dateMar 22, 2021
Quantity1088 units
LocationMirandola, N/A, Italy

Official product description

Spectrum Medical Quantum Standard heat exchanger

Why the product was recalled

Product labeled as sterile may not have been adequately sterilized. In addition, these devices were imported to the US distributor, but the devices are not 510(k) cleared in the US.

Distribution information

US Nationwide distribution in the state of South Carolina.

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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