Recall Register

Food, drugs, devices › Firms

CP Medical Inc

FDA recalling firm · 3 enforcement events · 3 product records · 2017–2019 · GA

CP Medical Inc has 3 FDA enforcement events on this register (3 product records) between 2017 and 2019: 3 device; the busiest year was 2019 with 2.

0% of its events are Class I; the most common class is Class II (3). 3 events are listed as ongoing; the recalling firm's address is in GA.

Recall classification reflects the relative degree of health hazard. Event counts depend on a firm's size and product range; they are not a comparison of one firm with another.

Enforcement events

InitiatedProduct (first record)TypeClassRecordsStatus
18 Oct 2019Coated PGA Undyed Polyglycolic Acid Braided Absorbable Suture Sterile EO 18" (45cm); UDI: (01)10790986000657 (17)220430 (10)17050970DeviceClass II1Ongoing
4 Feb 2019Plain and Chromic Gut Absorbable Surgical Sutures, sterile. 12 sutures per box. Product Usage: Plain Gut Sutures are indicated for use in general soft tissue approximation and/or ligation, including use in ophthalmic procedures, but not for use in cardiovascular and neural tissues.DeviceClass II1Ongoing
2 Feb 2017PGCL [poly (glycolide-co-caprolactone)] Absorbable Suture, Manufacturer CP Medical, Portland OR, Sterile, Product Codes L923, L459, L493, L762, L463, L922, L495, L463, L497, L494, L493DeviceClass II1Ongoing

By type and class

Device3
Class II3

Class I: 0% of this firm's events; 18% of all events on the register.

Events by year

17
18
19
20
21
22
23
24
25
26
Enforcement events for CP Medical Inc by year initiated.

Questions and answers

How many FDA recalls has CP Medical Inc had?

3 enforcement events (3 product records) on this register, 2017–2019: 3 device.

Are any CP Medical Inc recalls ongoing?

3 events are listed as ongoing in the current openFDA export.

What class are CP Medical Inc recalls?

3 Class II. 0% are Class I against 18% of all events on the register. Class reflects the relative degree of health hazard of the product, not the firm.

Where does this data come from?

openFDA food, drug and device enforcement reports (CC0), export dated 28 Sep 2026.

Provenance

Source: openFDA enforcement reports (CC0), export dated 28 Sep 2026. Firm names are grouped exactly as FDA spells them; the same company can appear under several spellings. Only organisations are shown. See the methodology.