Pneupac paraPac plus 300 ventilator kit, REF P300NGB
Reported: November 3, 2021 Initiated: July 15, 2021 #Z-0163-2022
Product Description
Pneupac paraPac plus 300 ventilator kit, REF P300NGB
Reason for Recall
Two devices were labeled with the same serial number
Details
- Recalling Firm
- Smiths Medical ASD Inc.
- Units Affected
- 2 units
- Distribution
- UK
- Location
- Minneapolis, MN
Frequently Asked Questions
What product was recalled? ▼
Pneupac paraPac plus 300 ventilator kit, REF P300NGB. Recalled by Smiths Medical ASD Inc.. Units affected: 2 units.
Why was this product recalled? ▼
Two devices were labeled with the same serial number
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on November 3, 2021. Severity: Low. Recall number: Z-0163-2022.
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