# FDA recall Z-0726-2024

> **Limacorporate S.p.A** · Class II · device recall initiated 2023-08-29.

## Product

PRIMA TT Glenoid Monoblock/Modular reverse TT baseplates: Description/Product Code:  BASEPLATE D.25MM REGULAR/1975.14.500,  BASEPLATE D.28MM REGULAR/1975.14.800,  BASEPLATE D.25MM FULL WEDGED 10-degrees/1975.14.510,  BASEPLATE D.28MM FULL WEDGED 10-degrees/1975.14.810,  BASEPLATE D.25MM FULL WEDGED 15-degrees/1975.14.615,  BASEPLATE D.28MM FULL WEDGED 15-degrees/1975.14.815,  BASEPLATE D.28MM FULL WEDGED 15-degrees X/1975.14.865,  BASEPLATE D.25 MM FULL WEDGED 20-degrees/1975.14.620,  BASEPLATE D.28 MM FULL WEDGED 20-degrees/1975.14.820,  BASEPLATE D.28 MM FULL WEDGED 20-degrees X/1975.14.870

## Reason for recall

Potential for baseplate peripheral holes to be out of specification due to a manufacturing issue, which could lead to loosening of the implant, or the screw moving from its original position.

## Distribution

US: IL, MO, CA, IN, MI, OK

## Key facts

- **Recall number:** Z-0726-2024
- **Recalling firm:** Limacorporate S.p.A
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-08-29
- **Report date:** 2024-01-24

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** San Daniele Del Friuli, N/A, Italy

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0726-2024

## Citation

> AI Analytics. FDA recall Z-0726-2024. Retrieved 2026-06-24 from https://api.ai-analytics.org/recall/Z-0726-2024. Source: US FDA. Licensed CC0.

---

*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*