FDA recall record

Abbott Laboratories WorkMate Claris v.1.2 Upgrade Kits, Model Numbers H800007 and H800012 recall — FDA Z-1855-2021

Due to a software error, the user may lose functionality of the system or the screen may turn black during operation.

Class IIclassification
Z-1855-2021official record ID
Jun 23, 2021report date

Recall record at a glance

Official recordZ-1855-2021
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmAbbott Laboratories Inc. (St Jude Medical)
Report dateJun 23, 2021
Recall initiation dateMay 5, 2021
Quantity8 units
LocationSaint Paul, MN, United States

Official product description

WorkMate Claris v.1.2 Upgrade Kits, Model Numbers H800007 and H800012

Why the product was recalled

Due to a software error, the user may lose functionality of the system or the screen may turn black during operation.

Distribution information

US Nationwide distribution in the states of MI, KS, MO, TX.

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: Visit.

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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