FDA recall record

Medica EasyCAL HbA1c Calibrator recall — FDA Z-1267-2018

Patient results determined using this calibrator lot might deviate up to 20%. Controls might not indicate false values.

Class IIclassification
Z-1267-2018official record ID
Apr 4, 2018report date

Recall record at a glance

Official recordZ-1267-2018
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmMedica Corporation
Report dateApr 4, 2018
Recall initiation dateApr 11, 2017
LocationBedford, MA, United States

Official product description

EasyCAL HbA1c Calibrator; REF 10658 Kit is packaged in a paper box containing 4 vials of 0.25ml of calibrant, one for each calibration level, and an insert sheet.

Why the product was recalled

Patient results determined using this calibrator lot might deviate up to 20%. Controls might not indicate false values.

Distribution information

USA: MI FL CA TX India, Russia, Puerto Rico, N. Mariana Island/Palau.

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: Letter.

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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