# FDA recall Z-2128-2026

> **Medline Industries, LP** · Class II · device recall initiated 2026-01-07.

## Product

Medline Surgical Drapes:  1) SHEET,DRAPE,40X58,STERILE, Model Number: DYNJP2410;   2) DRAPE,SHEET,ECONOMY,40X58",ST,20/CS, Model Number: DYNJP2411;   3) SHEET,DRAPE, 40X70,STERILE, Model Number: DYNJP2412;   4) DRAPE,MEDIUM,TAPE,40X70",ST,50/CS, Model Number: DYNJP2412T;   5) SHEET,DRAPE,53X77,STERILE, Model Number: DYNJP2414;   6) DRAPE,SHEET,3/4,53X77",ST,20/CS, Model Number: DYNJP2414R;   7) DRAPE,SHEET,ULTRAGARD,20/CS, Model Number: DYNJP2414UG;   8) DRAPE,RNF,53X77",ST,20/CS, Model Number: DYNJP2416;   9) SHEET,DRAPE,70X85,STERILE, Model Number: DYNJP2417;   10) DRAPE,FILM SHEET,44X65",ST,20/CS, Model Number: DYNJP2418;   11) DRAPE,SHEET,70X100",ST,12/CS, Model Number: DYNJP2419;   12) LEGGINGS,33X49",XL,PAIR,ST,CLR,20/CS, Model Number: DYNJP2462;   13) DRAPE,CHEST,FENESTRATION,15X10",ST,12/CS, Model Number: DYNJP2491;   14) DRAPE,MINOR PROC,6X6" FEN, ST,10/CS, Model Number: DYNJP2492;   15) SHEET, DRAPE, SPLIT, ST,10/CS, Model Number: DYNJP2498;   16) DRAPE,LAPAROTOMY,T-SHEET,ST,12/CS, Model Number: DYNJP3003;   17) DRAPE,LAPAROTOMY,T,ULTRAGARD,12/CS, Model Number: DYNJP3003UG;   18) DRAPE,LAPAROTOMY,POUCH,ST,12/CS, Model Number: DYNJP3008;   19) DRAPE,LAPAROTOMY,POUCH ULTRAGARD,12/CS, Model Number: DYNJP3008UG;   20) DRAPE,LAPAROTOMY,T,PEDIATRIC,ST,10/CS, Model Number: DYNJP3009;   21) DRAPE,LAPAROTOMY,ABDOMINAL,ST,12/CS, Model Number: DYNJP3101;   22) DRAPE,LAPROSCOPY,CHOLE,W/TROUGH,ST,8/CS, Model Number: DYNJP3102A;   23) DRAPE,LAP,CHOLE,W/TROUGH ULTRAGARD,12/CS, Model Number: DYNJP3102UG;   24) DRAPE,ABDOMINAL,MAJOR,ST,8/CS, Model Number: DYNJP3103;   25) DRAPE,ABDOMINAL,MAJOR,PCH/TRGH,ST,8/CS, Model Number: DYNJP3109;   26) DRAPE,TOP,102X53",ST,14/CS, Model Number: DYNJP4002;   27) DRAPE,CARDIOVASCULAR,SPLIT,ST,8/CS, Model Number: DYNJP4003;   28) DRAPE,ANGIO,BRACH,ECLIPSE,38X44,ST,40/CS, Model Number: DYNJP4106;   29) DRAPE,FEMORAL ANGIOGRAPHY,W/POUCH,8/CS, Model Number: DYNJP4119;   30) DRAPE,TOP,ARMCOVERS,106X59,STERILE,20/CS, Model Number: DYNJP4215;   31) DRAPE,UNDERBUTTOCK,PCH,ST,20/CS, Model Number: DYNJP6002;   32) DRAPE,UNDERBUTTOCK,GRAD POUCH,PORT,20/CS, Model Number: DYNJP6006;   33) DRAPE,EENT,SPLIT,ST,8/CS, Model Number: DYNJP7001;   34) SHEET,T,THYROID,ST,12/CS, Model Number: DYNJP7003;   35) DRAPE,EXTREMITY,89X128",ST,12/CS, Model Number: DYNJP8002;   36) DRAPE,EXTREMITY,ULTRAGARD,12/CS, Model Number: DYNJP8002UG;   37) T-DRAPE,EXTREMITY,ST,6/CS, Model Number: DYNJP8003;   38) T-DRAPE,EXTREMITY,ULTRAGARD,6/CS, Model Number: DYNJP8003UG;   39) DRAPE,HAND,ST,18/CS, Model Number: DYNJP8005;   40) DRAPE,HAND,ULTRAGARD,18/CS, Model Number: DYNJP8005UG;   41) DRAPE,HIP,W/POUCH,ST,5/CS, Model Number: DYNJP8201;   42) DBD-DRAPE,HIP,W/POUCHES, ULTRAGARD, Model Number: DYNJP8201UG;   43) DRAPE,ORTHOMAX,HIP,W/POUCH,6/CS, Model Number: DYNJP8211;   44) SHEET,ORTHO,SPLIT,ST,10/CS, Model Number: DYNJP8301;   45) DRAPE,SPLIT,77X120",10/CS, Model Number: DYNJP8304A;   46) ULTRAGARD SPLIT DRAPE,10/CS, Model Number: DYNJP8304UG;   47) DRAPE,SHOULDER,BEACH CHAIR,ST,5/CS, Model Number: DYNJP8412;   48) DRAPE,SHOULDER,BEACH CH,ULTRAGARD,5/CS, Model Number: DYNJP8412UG;   49) DRAPE,SHOULDER,BEACH CHAIR,ST,5/CS, Model Number: DYNJP8414;   50) DRAPE,LITHOTOMY,ST,8/CS, Model Number: DYNJP9001;   51) DRAPE,LAVH,ST,8/CS, Model Number: DYNJP9103;   52) DRAPE,VETERINARY,CUSTOM,SM,20/CS, Model Number: MED901;   53) DRAPE,VETERINARY,CUSTOM,M,20/CS, Model Number: MED902;   54) DRAPE,VETERINARY,CUSTOM,L,20/CS, Model Number: MED903

## Reason for recall

Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packaging cycles; however, the identified calibration issues have the potential to impact the sterility assurance level (SAL) of the Recalled Products.

## Distribution

Worldwide - US Nationwide distribution.

## Key facts

- **Recall number:** Z-2128-2026
- **Recalling firm:** Medline Industries, LP
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2026-01-07
- **Report date:** 2026-05-13

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Northfield, IL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2128-2026

## Citation

> AI Analytics. FDA recall Z-2128-2026. Retrieved 2026-06-14 from https://api.ai-analytics.org/recall/Z-2128-2026. Source: US FDA. Licensed CC0.

---

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