regard TOTAL HIP ARTHROPLASTY A&B, OR00032W, Item Number 880028023; ortho surgery convenience kit
Reported: November 30, 2022 Initiated: October 20, 2022 #Z-0304-2023
Product Description
regard TOTAL HIP ARTHROPLASTY A&B, OR00032W, Item Number 880028023; ortho surgery convenience kit
Reason for Recall
Surgical convenience kits were distributed containing 3M surgical drapes which were subsequently recalled.
Details
- Recalling Firm
- ROi CPS LLC
- Units Affected
- 125 kits
- Distribution
- LA, MO, NC, FL
- Location
- Republic, MO
Frequently Asked Questions
What product was recalled? ▼
regard TOTAL HIP ARTHROPLASTY A&B, OR00032W, Item Number 880028023; ortho surgery convenience kit. Recalled by ROi CPS LLC. Units affected: 125 kits.
Why was this product recalled? ▼
Surgical convenience kits were distributed containing 3M surgical drapes which were subsequently recalled.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on November 30, 2022. Severity: Moderate. Recall number: Z-0304-2023.
Related Recalls
FDA Devices Moderate
Convenience Kits 1. 25GA Convenience Kit - FNX VS0644.25-FNX 2. 25GA Convenience Kit - FXX VS0644.25-FXX 3.2…
Vortex Surgical Inc. · 2026-02-11
FDA Devices Moderate
COULTER DxH Diluent, REF 628017 COULTER DxH ECO Diluent REF C67250 For use as an isotonic buffered diluent in conju…
Beckman Coulter, Inc. · 2026-02-11
FDA Devices Moderate
Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number: KD-V411M-1520 Product Description: These inst…
Olympus Corporation of the Americas · 2026-02-11
FDA Devices Moderate
Product Name: Disposable Triple Lumen Sphincterotome Model/Catalog Number: KD-401Q-0330 Product Description: These in…
Olympus Corporation of the Americas · 2026-02-11
FDA Devices Moderate
Product Name: Lumipulse pTau 217 Plasma Controls Model/Catalog Number: 81558 Software Version: Not Applicable Produc…
Fujirebio Diagnostics, Inc. · 2026-02-11