Medline medical procedure kits labeled as follows: DENTAL, REF DYNJ909211A
Reported: August 28, 2024 Initiated: March 22, 2024 #Z-2702-2024
Product Description
Medline medical procedure kits labeled as follows: DENTAL, REF DYNJ909211A
Reason for Recall
A slight dimensional variation which has the potential for increased difficulty fitting into outer canister.
Details
- Recalling Firm
- MEDLINE INDUSTRIES, LP - Northfield
- Units Affected
- 99 units
- Distribution
- Worldwide - US Nationwide and the countries of Panama, Mexico, Canada, Qatar, El Salvador, Oman, Colombia, Singapore.
- Location
- Northfield, IL
Frequently Asked Questions
What product was recalled? ▼
Medline medical procedure kits labeled as follows: DENTAL, REF DYNJ909211A. Recalled by MEDLINE INDUSTRIES, LP - Northfield. Units affected: 99 units.
Why was this product recalled? ▼
A slight dimensional variation which has the potential for increased difficulty fitting into outer canister.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on August 28, 2024. Severity: Moderate. Recall number: Z-2702-2024.
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