Fresh Recalls

FDAClass II · Medical device · Recall Z-2308-2026 · Recalled June 10, 2026

TITANIUM/FLUOROPLASTIC PISTON 0 recall — Grace Medical, Inc.

Agency report date: June 10, 2026.

1. Compare your item

This notice names a product; your particular item is not yet verified. Compare every applicable model, serial, lot, production-date or model-year boundary below.

Product named
TITANIUM/FLUOROPLASTIC PISTON 0
Company / brand
Grace Medical
Lot / serial / date codes
Model/Catalog Number: 409-375 UDI code: (01)00844505000772(10)122927(17)310301 Lot Number: 122927
Distribution
U.S Nationwide distribution in the state of MD.
Agency product description and boundaries

TITANIUM/FLUOROPLASTIC PISTON 0.6MM DIA X 3.75MM L Model/Catalog Number: 409-375 Product Description: Stapes Prosthesis

Still to verify: match the label on your item with the full official notice, including any exclusions, tables and photos. Some identifiers appear only on the agency website and are absent from this data feed. A missing field does not mean all versions are affected.

If your lot or date falls outside a stated range, this notice has not established that your item is affected. This is not a finding about other recalls or product safety.

2. Agency hazard and consumer action

FDA reports: Due to incorrect functional length on device labeling.

No consumer remedy instructions are supplied in this record. Check the official notice and listed company contact for the agency’s current instructions.

Class II: may cause temporary or medically reversible health consequences.

Affected product: TITANIUM/FLUOROPLASTIC PISTON 0 recall status

3. Open the official notice or contact

Official recall ID
Z-2308-2026
Brand
All Grace Medical recalls
Classification
Class II
Units affected
7
Recall status
Ongoing
Initiated
Voluntary: Firm initiated

Affected products

Companies & origin

Recalling firm location
Bartlett, TN, United States
Firm address
8500 Wolf Lake Dr Ste 110, 38133-4104

Identifying details (verbatim from the notice)

Product codes / lots
Model/Catalog Number: 409-375 UDI code: (01)00844505000772(10)122927(17)310301 Lot Number: 122927
Distribution
U.S Nationwide distribution in the state of MD.
Firm notified the public via
Letter
FDA event ID
98773
Recall initiated
April 3, 2026
FDA classified
June 4, 2026
FDA report date
June 10, 2026

Other medical device recalls from around the same time

Verify with the official sources:

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Source: U.S. Food & Drug Administration. Agency excerpts come from the public data feed and may omit tables or later changes; the linked government source is authoritative. Source last checked October 22, 2026 at 6:00 PM UTC. Record retrieved September 8, 2026 at 6:00 PM UTC.

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