Brand Name: recall status

⚠ Recalls found. Brand Name is named in 5 official recalls in our current data:

FDA Class II recall Z-2822-2026 — Potential for Bar Code Reader (BCR) wands, used with the GEM Premier 5000 and GEM Premier 7000 systems, to assign patient results to an incorrect patient ID.
FDA Class II recall Z-2823-2026 — Potential for Bar Code Reader (BCR) wands, used with the GEM Premier 5000 and GEM Premier 7000 systems, to assign patient results to an incorrect patient ID.
FDA Class II recall Z-2824-2026 — Potential for Bar Code Reader (BCR) wands, used with the GEM Premier 5000 and GEM Premier 7000 systems, to assign patient results to an incorrect patient ID.
And 2 more listed below.

Brand: Instrumentation Laboratory

Recalls naming this model

FDA Class II · Medical device · August 5, 2026

Brand Name recall — Instrumentation Laboratory

Potential for Bar Code Reader (BCR) wands, used with the GEM Premier 5000 and GEM Premier 7000 systems, to assign patient results to an incorrect patient ID.

Company / brand: Instrumentation Laboratory

Affected product: Brand Name

Official ID Z-2822-2026 · Official record ↗

FDA Class II · Medical device · August 5, 2026

Brand Name recall — Instrumentation Laboratory

Potential for Bar Code Reader (BCR) wands, used with the GEM Premier 5000 and GEM Premier 7000 systems, to assign patient results to an incorrect patient ID.

Company / brand: Instrumentation Laboratory

Affected product: Brand Name

Official ID Z-2823-2026 · Official record ↗

FDA Class II · Medical device · August 5, 2026

Brand Name recall — Instrumentation Laboratory

Potential for Bar Code Reader (BCR) wands, used with the GEM Premier 5000 and GEM Premier 7000 systems, to assign patient results to an incorrect patient ID.

Company / brand: Instrumentation Laboratory

Affected product: Brand Name

Official ID Z-2824-2026 · Official record ↗

FDA Class II · Medical device · August 5, 2026

Brand Name recall — Instrumentation Laboratory

Potential for Bar Code Reader (BCR) wands, used with the GEM Premier 5000 and GEM Premier 7000 systems, to assign patient results to an incorrect patient ID.

Company / brand: Instrumentation Laboratory

Affected product: Brand Name

Official ID Z-2825-2026 · Official record ↗

FDA Class II · Medical device · August 5, 2026

Brand Name recall — Instrumentation Laboratory

Potential for Bar Code Reader (BCR) wands, used with the GEM Premier 5000 and GEM Premier 7000 systems, to assign patient results to an incorrect patient ID.

Company / brand: Instrumentation Laboratory

Affected product: Brand Name

Official ID Z-2826-2026 · Official record ↗

See all Instrumentation Laboratory recalls →

Verify with the official sources:

CPSC — consumer products ↗ (aggregated here)
NHTSA — vehicles, car seats, tires ↗ (aggregated here; use NHTSA's VIN lookup to check a specific vehicle)
FDA — food, drugs, medical devices ↗ (aggregated here)
USDA FSIS — meat, poultry & processed egg products ↗ (not aggregated here)
Recalls.gov — the U.S. government’s all-agency portal ↗

Found something wrong or missing? Report a data error.

Compiled from connected official public-domain government data. Sources last checked September 7, 2026 at 6:00 AM UTC.