Capillary mixing fleas recalled over an inadequate quality system
ASP Global is recalling 50,250 mixing fleas for SAFE-T-FILL blood gas capillaries over an inadequate quality system with unvalidated processes.
What this means for you
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: Scored 2 because the record cites a quality system and process validation finding rather than an identified defect or reported harm.
Plain-English summary
Mixing Fleas for SAFE-T-FILL Blood Gas Capillaries, model 07 9503, from ASP Global doing business as Anatomy Supply Partners, are being recalled.
The recall follows products manufactured under an inadequate quality system, including unvalidated manufacturing processes.
The recall covers 50,250 units carrying UDI-DI 10643351000366, across all lots produced from a stated start date. The product was distributed nationwide in the United States and in Canada. The FDA has classified the action as Class II.
The enforcement record cites the quality system finding without describing a device defect or health consequence, and reports no injuries. Laboratories holding affected stock should follow the firm's instructions.
The recalled product
- Product
- Mixing Fleas for SAFE-T-FILL Blood Gas Capillaries, Model 07 9503
- Manufacturer
- ASP Global, LLC. dba Anatomy Supply Partners, LLC.
- Hazard
- quality-system
- unvalidated-process
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (10)
- 22E4465
- 22I4072
- 23B4158
- 23C4345
- 23F4176
- 23H4109
- 23I4060
- 24D4021
- 24E4130
- 24E4131
Distribution
Distributed nationwide across the United States.
Related recalls
Same category
- HighMedtronic DLP One-Piece Pediatric Arterial Cannula Recalled for Foreign Material
FDA (Devices) · 2026-07-22
- SevereAbiomed Impella CP Smart Assist Set Heart Pump Introducer Sheath Leakage
FDA (Devices) · 2026-07-22
- SevereMedtronic Bio-Medicus Adult Cannula Kit Recalled for Foreign Material
FDA (Devices) · 2026-07-22
- HighVasoview Hemopro 2 Endoscopic Vessel Harvesting System Recall
FDA (Devices) · 2026-07-22
- HighMobile Digital Radiographic System Arm Drop Risk During Patient Exams
FDA (Devices) · 2026-07-22