The Recall Desk

Hazard

Adhesive Residue recalls

16 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.

What the numbers show

Total
16
Critical
0
Severe
0
Most recent
2026-10-28

Of the 16 adhesive residue recalls we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 0 (0%) are Severe.

About this hazard tag

Hazard tags are short, machine-readable labels we attach to every recall to make cross-cutting queries possible — “all adhesive residue recalls regardless of agency”, “all listeria recalls in California”, “all airbag recalls in 2025”. The tags are extracted from each recall’s source text during the LLM rewrite step and validated against a fixed schema.

A recall can carry multiple tags — a Listeria recall might also be tagged ready-to-eat and undeclared-allergen. Use the full-text search if you want to combine hazard tags with brand or category filters.

1–16 of 16

  • ModerateFDA (Devices)·Z-0277-2027·2026-10-28

    Medline Medical Convenience Kits Recalled for Adhesive Removal Issues

    Medline Industries is recalling specific medical convenience kits because they are difficult to remove and leave adhesive residue on patient skin.

    Product
    MEDLINE medical convenience kits labeled as: 1) LAPAROTOMY GYN CDS, Medline Kit Number/SKU CDS983529O; 2) GYN ROBOTIC PK-LF, Medline Kit Number/SKU DYNJ52432M; 3) TAH PACK, Medline Kit Number/SKU DYNJ60646A; 4) TUBAL LIGATION RFD, Medline Kit Number/SKU DYNJ906291F.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0280-2027·2026-10-28

    Medline C-Section Tray Kits Recalled for Adhesive Removal Issues

    Medline is recalling 108 C-Section Tray kits because they are difficult to remove from patients and leave adhesive residue on the skin.

    Product
    MEDLINE medical convenience kits labeled as: C-SECTION TRAY-LF, Medline Kit Number/SKU OBN471K
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0272-2027·2026-10-28

    Medline FETOSCOPY CDS-LF Kits Recalled for Adhesive Removal Issues

    Medline Industries is recalling 10 FETOSCOPY CDS-LF medical convenience kits because they are difficult to remove from patients and leave adhesive residue on the skin.

    Product
    MEDLINE medical convenience kits labeled as: FETOSCOPY CDS-LF, Medline Product Number/SKU CDS840215P
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0275-2027·2026-10-28

    Medline Medical Convenience Kits Recalled for Adhesive Removal Issues

    Medline Industries is recalling 26,965 medical convenience kits because they are difficult to remove from patients and leave adhesive residue on the skin.

    Product
    MEDLINE medical convenience kits labeled as (list truncated)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0281-2027·2026-10-28

    Medline Recalls Hip Scope Packs Due to Removal Difficulties

    Medline Industries is recalling 56 hip scope packs because they are difficult to remove and leave adhesive residue on patient skin.

    Product
    MEDLINE medical convenience kits labeled as: 1) HIP SCOPE PACK, Medline Kit Number/SKU DYNJ64103C; 2) HIP SCOPE PACK, Medline Kit Number/SKU DYNJ64155B.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0271-2027·2026-10-28

    Medline C-Section Drapes Recalled for Adhesive Removal Issues

    Medline Industries is recalling C-section drapes that are difficult to remove and leave adhesive residue on patient skin.

    Product
    MEDLINE DRAPE C-SECTION FEN CLR SCREEN W, Medline Product Number/SKU DYNJP6108
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0276-2027·2026-10-28

    Medline Medical Convenience Kits Recalled for Adhesive Removal Issues

    Medline Industries is recalling 2,229 medical convenience kits because they are difficult to remove from patients and leave adhesive residue on the skin.

    Product
    MEDLINE medical convenience kits labeled as: 1) BIRTHDAY KIT-DOUBLE BASIN-LF, Medline Kit Number/SKU DYNJ16127N; 2) NYGH-DELIVERY PACK-LF, Medline Kit Number/SKU DYNJ27206D; 3) OB/GYN, Medline Kit Number/SKU DYNJ911652.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0279-2027·2026-10-28

    Medline Tubal Ligation Kits Recalled for Adhesive Removal Issues

    Medline Industries is recalling three tubal ligation kits because they are difficult to remove from patients and leave adhesive residue on the skin.

    Product
    MEDLINE medical convenience kits labeled as: TUBAL LIGATION RFD, Medline Product Number/SKU DYNJ906291G
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0270-2027·2026-10-28

    Medline Drape C-SEC Fen Clear Screen Wire Recall

    Medline Industries is recalling 161 units of Drape C-SEC Fen Clear Screen Wire because the product is difficult to remove and leaves adhesive residue on patient skin.

    Product
    MEDLINE DRAPE C-SEC FEN CLEAR SCRN WIRE, Medline Product Number/SKU DYNJP6106
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0273-2027·2026-10-28

    Medline C-Section Pack Recall for Adhesive Removal Issues

    Medline is recalling 222 C-Section Pack kits because they are difficult to remove and leave adhesive residue on patient skin.

    Product
    MEDLINE medical convenience kits labeled as: C-SECTION PACK, Medline Product Number/SKU DYNJ48455A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0269-2027·2026-10-28

    Medline C-Section Drapes Recalled for Adhesive Removal Issues

    Medline Industries is recalling C-section drapes with pouches because they are difficult to remove and leave adhesive residue on patient skin.

    Product
    MEDLINE DRAPE C-SECTION W/POUCH ST 7/CS, Medline Product Number/SKU DYNJP6101
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0274-2027·2026-10-28

    Medline Medical Convenience Kits Recalled for Adhesive Removal Issues

    Medline Industries is recalling 233 medical convenience kits because they are difficult to remove from patients and leave adhesive residue on the skin.

    Product
    MEDLINE medical convenience kits labeled as: 1) FETAL SURGERY CDS-LF, Medline Kit Number/SKUCDS840214R; 2) MAJOR, Medline Kit Number/SKUDYNJ904851I; 3) ABDOMINAL TRANSPLANT, Medline Kit Number/SKUDYNJ908124B.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1017-2022·2022-05-04

    Empower Introducer Sheath recalled for potential embolism and ischemia risk

    Freudenberg Medical is recalling Empower Introducer Sheath devices (Model 668782-200) due to potential adhesive residue inside the catheter shaft that may cause blood clots and tissue damage. Affected devices were distributed in the US and Netherlands.

    Product
    Empower Introducer Sheath with Hydrophilic Coating 21F x 56cm Model: 668782-200 (OUS)
    Category
    Medical Device
    Distribution
    2 states
  • HighFDA (Devices)·Z-0632-2022·2022-02-16

    Orthopedic knee replacement component recalled for adhesive residue contamination

    DePuy Orthopaedics is recalling 3 units of ATTUNE REVISION DISTAL FEMORAL AUGMENT due to adhesive residue that could cause tissue irritation or infection if not detected before surgery.

    Product
    ATTUNE REVISION DISTAL FEMORAL AUGMENT SZ 6 4MM- Intended as a Component in total knee arthroplasty (TKA) revision surgeries Product Number: 154706001
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0631-2022·2022-02-16

    Knee Replacement Component Recalled for Adhesive Residue Risk

    DePuy Orthopaedics is recalling ATTUNE Revision knee implant components due to possible adhesive residue on the surface. If undetected before surgery, the residue may cause soft tissue irritation or infection.

    Product
    ATTUNE REVISION POSTERIOR FEMORAL AUGMENT SZ 9 12MM-intended as a Component in total knee arthroplasty (TKA) revision surgeries Product Number: 154909003
    Category
    Medical Device
    Distribution
    Distributed nationwide