FDA recall record

Stryker recall — FDA Z-1428-2021

Their is a potential that Video Processor/Illuminators may exhibit flickering, loss of image or unintended reboots.

Class IIclassification
Z-1428-2021official record ID
Apr 21, 2021report date

Recall record at a glance

Official recordZ-1428-2021
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmStryker Corporation
Report dateApr 21, 2021
Recall initiation dateFeb 26, 2021
Quantity125 units
LocationSan Jose, CA, United States

Official product description

Stryker, REF PC9001, PINPOINT Video Processor/Illuminator, Rx Only CE 0197, MD Medical Device, UDI: (01) 00858701006049 - Product Usage: used with both the SPY-PHI and PINPOINT systems, the intended use for both imaging systems are being documented here.

Why the product was recalled

Their is a potential that Video Processor/Illuminators may exhibit flickering, loss of image or unintended reboots.

Distribution information

Worldwide distribution - US Nationwide distribution including in the states of CA, CO, FL, IL, MA MI, MS NC, NV, OK, PA, SC, TN, TX, VA, WA, WI and the countries of AE, CA, CN, CZ, DE, ES, HK, JP, KR, KW, MX, MY, PH, RO, SG, TR, TW.

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

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