Aspen Surgical Products, Inc.
6945 SOUTHBELT DR. S.E., Caledonia, MI, US
Registered product codes
655 product codes
Recent MDR events
633 on file
- RapidClean® Rongeur, 40° Up, Ceramic Coated, Convertible, 3Jul 28, 2026Malfunction3002750084-2026-00080
- Symmetry® Rongeur, Decker Micro, Straight, 152 mmJul 28, 2026Malfunction3002750084-2026-00081
- Dr Fog Treated Sponge; SterileJul 28, 2026Malfunction3002750084-2026-00082
- RICHARD-ALLAN® NEEDLE 1/2 CIRCLE TAPERJul 22, 2026Malfunction25904376
- UNKNOWN, BUT IS A CODMAN RHOTON NERVE HOOKJul 16, 2026Malfunction3002750084-2026-00078
- BARD-PARKER SAFETYLOCK CARBON RIB-BACK BLADES SIZE 11, STERILEJul 15, 2026Malfunction3002750084-2026-00077
- BERKETTE BEACH CHAIR LIMB POSITIONER, STERILEJul 15, 2026Malfunction3002750084-2026-00075
- CAUTERY HIGH TEMP FINE TIPJul 14, 2026Malfunction3002750084-2026-00073
- NEEDLE 1/2 CIRCLE TAPER POINT MAYO CATGUT .050X0.897 STERILEJul 8, 2026Malfunction3002750084-2026-00071
- PROTEK; ENDOCAVITY PROBE COVER; 3.5CM X 20CM; LATEX; ROLLED; 4 BANDS; STERILEJul 8, 2026Malfunction3002750084-2026-00072
Recalls
33 on file
- TerminatedApr 7, 2014
The recall has been initiated due to a potential compromise of the sterile barrier of the Surgidyne Wound Drainage and Surgidyne Bulb Evacuator & Collection System medical devices.
View FDA record ↗ - TerminatedApr 7, 2014
The recall has been initiated due to a potential compromise of the sterile barrier of the Surgidyne Wound Drainage and Surgidyne Bulb Evacuator & Collection System medical devices.
View FDA record ↗ - TerminatedApr 7, 2014
The recall has been initiated due to a potential compromise of the sterile barrier of the Surgidyne Wound Drainage and Surgidyne Bulb Evacuator & Collection System medical devices.
View FDA record ↗ - TerminatedApr 7, 2014
The recall has been initiated due to a potential compromise of the sterile barrier of the Surgidyne Wound Drainage and Surgidyne Bulb Evacuator & Collection System medical devices.
View FDA record ↗ - TerminatedApr 7, 2014
The recall has been initiated due to a potential compromise of the sterile barrier of the Surgidyne Wound Drainage and Surgidyne Bulb Evacuator & Collection System medical devices.
View FDA record ↗ - TerminatedApr 7, 2014
The recall has been initiated due to a potential compromise of the sterile barrier of the Surgidyne Wound Drainage and Surgidyne Bulb Evacuator & Collection System medical devices.
View FDA record ↗ - TerminatedApr 7, 2014
The recall has been initiated due to a potential compromise of the sterile barrier of the Surgidyne Wound Drainage and Surgidyne Bulb Evacuator & Collection System medical devices.
View FDA record ↗ - TerminatedApr 7, 2014
The recall has been initiated due to a potential compromise of the sterile barrier of the Surgidyne Wound Drainage and Surgidyne Bulb Evacuator & Collection System medical devices.
View FDA record ↗ - TerminatedApr 7, 2014
The recall has been initiated due to a potential compromise of the sterile barrier of the Surgidyne Wound Drainage and Surgidyne Bulb Evacuator & Collection System medical devices.
View FDA record ↗ - TerminatedApr 7, 2014
The recall has been initiated due to a potential compromise of the sterile barrier of the Surgidyne Wound Drainage and Surgidyne Bulb Evacuator & Collection System medical devices.
View FDA record ↗
Compliance history
Matched by FEI 3002750084.
FDA inspections
0 on file
No inspections on file for this FEI number.
Inspection citations
0 on file
No citations on file for this FEI number.
Compliance actions
0 on file
No warning letters or injunctions on file for this FEI number.
Import refusals
0 on file
No import refusals on file for this FEI number.