# FDA recall Z-2919-2026

> **Covidien, LP** · Class II · device recall initiated 2026-06-24.

## Product

V-Loc 180 Absorbable Wound Closure Device    BOX BEDSIDE STAPLING IS KING	  	BOX06614V4  	  BOX BY PASS FINAL	  	BOX07405V1  	  BOX BYPASS CARDON	  	BOX01056V2	  	  BOX BYPASS DR LAGAE	  	BOX01482V2  		  BOX BYPASS KIT DEZEMBER 2025	  	BOX09222V1  		  BOX BYPASS KIT NEU BOX 003	  	BOX08767V1  	  BOX GASTRIC BYPASS	  	JAWBYPASS2  	  BOX GASTRIC BYPASS SIGNIA	  	BOX02191V11    BOX GASTRICBYPASS KIT V4	  	BOX06863V4  	  BOX GB BOX MET LHOOK	  	PST04884V3    BOX GB ZONDER ENDOHERNIA EGIA	  	PST04884V6    BOX GBP SIGNIA	  	BOX08506V2    BOX KIT COLON IHS	  	KIT00625V1	  	  BOX KIT HERNIA HIATO IHS	  	KIT01026V1	  	  BOX LAP HERNIE INGUNIAL RIGHT	  	BOX00051V4    BOX NEW GBP KIT	  	PST03130V2    BOX ZESTAW DO BARIATRII GB	  	UCKGB5    BOX ZESTAW DO RYGB	  	WEJRYGB3    VLOCL0013 V-LOC* 180 4-0 CLR 30CM P12	  	VLOCL0013    VLOCL0014 V-LOC* 180 3-0 CLR 30CM P12	  	VLOCL0014    VLOCL0023 V-LOC* 180 4-0 CLR 45CM P12	  	VLOCL0023    VLOCL0024 V-LOC* 180 3-0 CLR 45CM P12	  	VLOCL0024    VLOCL0306 V-LOC 180 DEVICE 0 15CM GS-21	  	VLOCL0306    VLOCL0316 V-LOC* 180 0 GRN 30CM GS21X12	  	VLOCL0316  	  VLOCL0345 V-LOC* 180 2-0 GRN 23CM GS21	  	VLOCL0345    VLOCL0436 V-LOC* 180 0 GRN 60CM GS25X12	  	VLOCL0436    VLOCL0604 V-LOC* 180 3-0 GRN 15CM V20	  	VLOCL0604    VLOCL0615 V-LOC* 180 2-0 GRN 30CM V20	  	VLOCL0615  	  VLOCL0625 V-LOC* 180 2-0 GRN 45CM V20	  	VLOCL0625  	  VLOCL0644 V-LOC* 180 3-0 GRN 23CM V20	  	VLOCL0644  	  VLOCL0804 V-LOC 180 3-0 GRN 15CM CV23	  	VLOCL0804    VLOCL2105 V-LOC* 180 2-0 GRN 15CM GS22	  	VLOCL2105    VLOCL2145 V-LOC* 180 2-0 GRN 23CM GS22	  	VLOCL2145    VLOCL2246 VLOC180 0 GRN 9 GS-22	  	VLOCL2246

## Reason for recall

Product may contain a perforation or tear in the sterile barrier packaging. This issue may result in biocontamination of the sterile sutures, which may lead to infection, loss of vision if in ophthalmic utilization, or prolonged surgery.

## Distribution

US Nationwide and the countries of Australia, Austria, Belgium, Bulgaria, Canada, Canary Islands, Chile, China, Colombia, Croatia, Cyprus, Czech Republic, Denmark, Estonia, Finland, France, Germany, Greece, Guadeloupe, Guatemala, Honduras, Hong Kong, Hungary, Iceland, India, Ireland, Israel, Italy, Japan, Kosovo, Lebanon, Lithuania, Luxembourg, Mexico, Namibia, Netherlands, North Macedonia, Northern Ireland, Norway,  Oman, Panama, Poland, Portugal, Qatar, Reunion, Romania, Russia, Saudi Arabia, Singapore, Slovakia, Slovenia, South Africa, South Korea, Spain, Sweden, Switzerland,  Taiwan, Thailand, Ukraine, United Arab Emirates, United Kingdom, Uzbekistan.

## Key facts

- **Recall number:** Z-2919-2026
- **Recalling firm:** Covidien, LP
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2026-06-24
- **Report date:** 2026-08-19

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** North Haven, CT, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2919-2026

## Citation

> MORVS. FDA recall Z-2919-2026. Retrieved 2026-10-22 from https://api.morvs.ai/recall/Z-2919-2026. Source: US FDA. Licensed CC0.

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*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*