Home › ASPEN SURGICAL PRODUCTS, INC. › Richard-Allan® Vessel Loop
Richard-Allan® Vessel Loop
ASPEN SURGICAL PRODUCTS, INC. · Model 3901 · UDI-DI 00887761007239
10
510(k) clearances
866
Adverse events (2 deaths)
38
Recalls
228
Facilities
Description
Intended to be used to occlude, retract and identify arteries, veins, tendons and nerves in surgical procedures
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2025-04-09 | MEDLINE INDUSTRIES, LP - Northfield | Three is the potential for the retractors to puncture through the sterile packaging. |
| 2024-02-23 | MEDLINE INDUSTRIES, LP - Northfield | Product may have a weak seal which may result in a breach of sterility of the contents if the seal fails. The weak seal may not be detectable by all users. |
| 2022-10-12 | Medical Action Industries, Inc. 306 | Scissors contained debris. |
| 2021-05-11 | Medical Action Industries, Inc. 306 | There is a potential for flaking metal and/or brown spots on the hemostats sold as individual units or packaged in the kits |
| 2021-05-11 | Medical Action Industries, Inc. 306 | There is a potential for flaking metal and/or brown spots on the hemostats sold as individual units or packaged in the kits |
| 2016-08-01 | Ethicon, Inc. | ETHICON MERSILENE" Tape (also referred to as MERSILENETM Polyester Fiber Strip or MERSILENETM Fiber Ligature) products are being recalled since a group of MERSILENE" Tape product c |
| 2011-03-28 | Hospira Inc. | There is a potential for the air filter at the distal end of the set to become detached. This could result in the contamination of the sterile fluid path inside the tubing. |
| 2011-03-28 | Hospira Inc. | There is a potential for the air filter at the distal end of the set to become detached. This could result in the contamination of the sterile fluid path inside the tubing. |
| 2011-03-28 | Hospira Inc. | There is a potential for the air filter at the distal end of the set to become detached. This could result in the contamination of the sterile fluid path inside the tubing. |
| 2011-03-28 | Hospira Inc. | There is a potential for the air filter at the distal end of the set to become detached. This could result in the contamination of the sterile fluid path inside the tubing. |
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Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.