FDA recall record

Cochlear Baha 5 Sound Processor Tamper Proof Battery Door (3 pcs.) recall — FDA Z-0792-2020

Product was packaged with the Incorrect tamper proof battery door.

Class IIclassification
Z-0792-2020official record ID
Jan 15, 2020report date

Recall record at a glance

Official recordZ-0792-2020
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmCochlear Americas Inc.
Report dateJan 15, 2020
Recall initiation dateDec 18, 2018
Quantity50 units
LocationCentennial, CO, United States

Official product description

Cochlear Baha 5 Sound Processor Tamper Proof Battery Door (3 pcs.)

Why the product was recalled

Product was packaged with the Incorrect tamper proof battery door.

Distribution information

Domestic: CA, FL, IL, IN, MA, MO, NY, SD, TN, and TX OUS Regions; Asia Pacific (APAC), and Europe, The Middle East and Africa (EMEA)

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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