Centurion- Laceration Trays DYNDL1073 LACERATION TRAY DYNDL1152A LACERATION TRAY DYNDL1152A LACERATION TRAY…
Medical device recall Z-1053-2020. Published in FDA’s Enforcement Report on Feb 12, 2020.
No Watch here, and no alerts: openFDA asks that its enforcement data “should not be used as a method to collect data to issue alerts to the public, nor should it be used to track the lifecycle of a recall” (openFDA). For FDA’s own recall emails, subscribe at FDA. FDA’s own record is on accessdata.fda.gov.
The short answer
Published in FDA’s Enforcement Report on Feb 12, 2020. Copied from openFDA on Oct 20, 2026.
Every line below is in FDA’s own words, with its source beside it. FDA’s terms are explained in FDA’s own words.
How serious is it, by FDA’s class?
Class II, the middle of FDA’s three classes.
“Products that might cause a temporary health problem, or pose only a slight threat of a serious nature. Example: a drug that is under-strength but that is not used to treat life-threatening situations.”
openFDA, in plain words, its enforcement report fields.
“Class II is a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote.”
FDA’s rule, 21 CFR 7.3(m)(2), eCFR.
What these words mean is quoted from openFDA’s field reference and 21 CFR 7.3.
What’s wrong with it?
Incomplete seals on the sterile package may compromise the sterility
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Which ones are recalled?
Centurion- Laceration Trays DYNDL1073 LACERATION TRAY DYNDL1152A LACERATION TRAY DYNDL1152A LACERATION TRAY DYNDL1223A LACERATION TRAY DYNDL1295B KIT,PAIN DYNDL1436A LACERATION TRAY DYNDL1436A LACERATION TRAY DYNDL1600B RCHSD CVP TRAY DYNDL1606A VAGINAL DELIVERY TRAY DYNDL1617A PICC INSERTION KIT-LATEX FREE DYNDL1617A PICC INSERTION KIT-LATEX FREE DYNDL1630A LACERATION TRAY DYNDL1675 ARTHROGRAM TRAY DYNDL1721 LACERATION TRAY DYNDL1721 LACERATION TRAY DYNDL1741A LACERATION TRAY DYNDL1744 LACERATION KIT DYNDL1755 LACERATION TRAY DYNDL1764A LACERATION TRAY DYNDL1772 LACERATION TRAY DYNDL1772 LACERATION TRAY DYNDL1786 SUTURING SET DYNDL1790 LACERATION TRAY DYNDL1796 LACERATION TRAY DYNDL1812 PEDI LACERATION TRAY DYNDL1840 SUTURE SET PACK DYNDL1847 ER SUTURE TRAY DYNDL1864A LACERATION TRAY DYNDL1897 LACERATION TRAY DYNDL1897 LACERATION TRAY DYNDL1920 LACERATION TRAY
How much: “N/A”, in FDA’s words.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Codes to check against yours
Lot Numbers: DYNDL1073 LACERATION TRAY 2019011590 DYNDL1152A LACERATION TRAY 2018122790 DYNDL1152A LACERATION TRAY 2018092090 DYNDL1223A LACERATION TRAY 2018112190 DYNDL1295B KIT,PAIN 2018112690 DYNDL1436A LACERATION TRAY 2019010490…
Every code shown here, 1,199 characters
Lot Numbers: DYNDL1073 LACERATION TRAY 2019011590 DYNDL1152A LACERATION TRAY 2018122790 DYNDL1152A LACERATION TRAY 2018092090 DYNDL1223A LACERATION TRAY 2018112190 DYNDL1295B KIT,PAIN 2018112690 DYNDL1436A LACERATION TRAY 2019010490 DYNDL1436A LACERATION TRAY 2018122190 DYNDL1600B RCHSD CVP TRAY 2019030890 DYNDL1606A VAGINAL DELIVERY TRAY 2018112190 DYNDL1617A PICC INSERTION KIT-LATEX FREE 2019032190 DYNDL1617A PICC INSERTION KIT-LATEX FREE 2018120390 DYNDL1630A LACERATION TRAY 2019011090 DYNDL1675 ARTHROGRAM TRAY 2019021290 DYNDL1721 LACERATION TRAY 2019032590 DYNDL1721 LACERATION TRAY 2018100590 DYNDL1741A LACERATION TRAY 2018111390 DYNDL1744 LACERATION KIT 2018121790 DYNDL1755 LACERATION TRAY 2018121890 DYNDL1764A LACERATION TRAY 2018112190 DYNDL1772 LACERATION TRAY 2019051690 DYNDL1772 LACERATION TRAY 2018122190 DYNDL1786 SUTURING SET 2019022790 DYNDL1790 LACERATION TRAY 2019012590 DYNDL1796 LACERATION TRAY 2018101590 DYNDL1812 PEDI LACERATION TRAY 2019061090 DYNDL1840 SUTURE SET PACK 2019031490 DYNDL1847 ER SUTURE TRAY 2019051390 DYNDL1864A LACERATION TRAY 2018112790 DYNDL1897 LACERATION TRAY 2018121090 DYNDL1897 LACERATION TRAY 2018111990 DYNDL1920 LACERATION TRAY 2018101290
Copied exactly as FDA lists them: lot and serial numbers, dates and other codes on the product or its label.
Where did it go?
FDA’s words for the “general area of initial distribution”: where the firm first shipped it.
Nationwide Foreign: GHANA
These words name no state.
What FDA means by nationwide
“The term “nationwide” is defined to mean the fifty states or a significant portion. Note that subsequent distribution by the consignees to other parties may not be included.”
openFDA, its enforcement report fields.
The words say it went outside the United States too.
What these words mean is quoted from openFDA’s field reference and 21 CFR 7.3.
Is it still going on?
Terminated, in FDA’s file.
“FDA has determined that all reasonable efforts have been made to remove or correct the violative product in accordance with the recall strategy, and proper disposition has been made according to the degree of hazard.”
openFDA, on “Terminated”, its enforcement report fields.
What these words mean is quoted from openFDA’s field reference and 21 CFR 7.3.
- The firm began the recall on Dec 11, 2019.
- FDA classified it on Feb 5, 2020.
- FDA’s Enforcement Report published it on Feb 12, 2020.
- FDA terminated it on Sep 4, 2020.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Who is recalling it?
- Centurion Medical Products Corporation, of Williamston, MI.
- Who began it, in FDA’s words: Voluntary: Firm initiated.
- How the firm first told its customers: Letter.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
What this record can’t tell you
- Whether your own one is affected: compare the codes, dates and numbers above with yours. When unsure, ask the firm or the store.
- Where it went after the firm’s first shipments. FDA’s words cover the firm’s initial distribution, and, in FDA’s words, “subsequent distribution by the consignees to other parties may not be included.”
- How many have been returned, corrected or destroyed: FDA’s report doesn’t say.
- Whether anyone was hurt or fell ill: the report doesn’t say.
- How current it is: openFDA publishes FDA’s Enforcement Report weekly, after FDA does, and a firm can announce a recall weeks before it appears there. openFDA’s own caution: “This data should not be used as a method to collect data to issue alerts to the public, nor should it be used to track the lifecycle of a recall.”
- A product with no recall here isn’t safe by that: FDA’s report lists the recalls FDA classified, and when.
Hearth Record wrote these lines; the quotations are FDA’s.
Sources
-
U.S. Food and Drug Administration, Device recall enforcement reports.
Released Oct 14, 2026 and checked Oct 20, 2026. Updated weekly. Public domain (CC0 1.0, openFDA). FDA asks that nothing suggest it endorses this site.
Recalls of food, medicines, medical devices, pet food and animal drugs are from the U.S. Food and Drug Administration (FDA). FDA does not endorse Hearth Record. openFDA: “Do not rely on openFDA to make decisions regarding medical care.” Copied on Oct 20, 2026.