Exact FDA event identifier

Event 97275

2 recalled-product records grouped only because every row carries this exact official event ID.

Event summary

Timeline bucket: July 15, 2025
Product types: Device
Classifications: Class II
Statuses: Ongoing
Recalling firm wording: Waldemar Link GmbH & Co. KG (Mfg Site)

Dossier provenance

Source snapshots represented here

openFDA Device Enforcement Report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.
openFDA Device Recall event_date_initiated coverage June 01, 1997–June 30, 2026

Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.

How coverage and grouping work

Complete imported group

Every recalled product in this event

2 official enforcement rows

Product dates, classifications, firms, and source wording remain attached to their individual rows. Opening this dossier never hides products that did not match a prior timeline filter.

device · product 1 of 2

Prosthesis Head B, 28 mm, 7 mm neck length. Item Number: 198-828/04.

Z-2288-2025

Recall number: Z-2288-2025
Initiated: July 15, 2025
Classification: Class II
Status: Ongoing
Recalling firm: Waldemar Link GmbH & Co. KG (Mfg Site)
Quantity: 46 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0

Inconsistent size terminology and color coding used on labeling

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Inconsistent size terminology and color coding used on labeling

Code information

Item Number: 198-828/04. UDI-DI: 04026575193783. Serial Numbers: 211117/0069, 211117/0070, 211117/0071, 211117/0073, 211117/0078, 220204/0613, 220204/0614, 220204/0615, 220204/0616, 220204/0617, 220204/0618, 220204/0619, 220204/0620, 220204/0621, 220204/0622, 220204/0623, 220204/0624, 220204/0627, 220304/0074, 220304/0075, 220304/0076, 220304/0077, 220304/0078, 220304/0080, 220304/0081, 220304/0082, 220304/0083, 220517/0052, 220517/0069, 220517/0070, 220517/0071, 220517/0072, 220517/0073, 220517/0074, 220517/0076, 220517/0078, 220517/0079, 220517/0080, 220517/0081, 220517/0085, 220517/0088, 220517/0089, 220517/0090, 221011/0093, 240415/3890, 240415/3896.

Distribution pattern

Worldwide - US Nationwide distribution in the states of AZ, CA, FL, IN, KS, LA, NJ and the countries of Germany, Argentina, Belgium, Switzerland, Cyprus, Algeria, Finland, Hungary, Mexico, Netherlands, Peru, Slovenia, and Uruguay.

device · product 2 of 2

Plastic Trial Head Brown, 7 mm neck length. Item Number: 175-928/15.

Z-2289-2025

Recall number: Z-2289-2025
Initiated: July 15, 2025
Classification: Class II
Status: Ongoing
Recalling firm: Waldemar Link GmbH & Co. KG (Mfg Site)
Quantity: 17 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0

Inconsistent size terminology and color coding used on labeling

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Inconsistent size terminology and color coding used on labeling

Code information

Item Number: 175-928/15. UDI-DI: 04026575150700. Serial Numbers: C126168, C424053