The Recall Desk

Hazard

Latex Allergy recalls

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

What the numbers show

Total
108
Critical
0
Severe
2
Most recent
2020-07-22

Of the 108 latex allergy recalls we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2 (2%) are Severe.

Which agencies issued them

About this hazard tag

Hazard tags are short, machine-readable labels we attach to every recall to make cross-cutting queries possible — “all latex allergy 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.

1–25 of 108

  • ModerateFDA (Devices)·Z-2590-2020·2020-07-22

    DJO Nylatex Wraps Recalled for Missing Latex Warning Labels

    DJO, LLC is recalling Nylatex wraps used with Intelect and V-Sonic devices because they lack appropriate latex warning labels.

    Product
    This is an accessory to Intelect Advanced, Intelect Mobile, Intelect Neo, and V-Sonic devices. NYLATEX WRAP - Product Usage: are intended to be used based on the devices associated with them. Nylatex wraps are composed of nylon and natural rubber and are accessories used to secur
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0863-2020·2020-02-05

    Custom Healthcare Systems Recalls Inpatient Dialysis Kits Due to Latex

    Custom Healthcare Systems is recalling 240 inpatient dialysis kits because a component contains latex that was not listed on the product labels.

    Product
    Custom Healthcare Systems, Inc. Inpatient Dialysis Kit PAK-19244. Single use. Dialysis kit
    Category
    Medical Device
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-0026-2020·2019-10-09

    Merit Medical Systems Recalls Custom Procedure Kits Due to Latex Labeling Error

    Merit Medical Systems is recalling 88 Custom Procedure Kits because they were incorrectly labeled as latex-free.

    Product
    Custom Procedure Kit, Custom Kit, REF/Product Code: K12T-03688, single use, RX Only, Sterile EO, LATEX FREE, UDI: (01)00884450389409
    Category
    Medical Device
    Distribution
    2 states
  • HighFDA (Devices)·Z-1285-2019·2019-05-15

    Cardinal Health Recalls ChemoPlus Goggles Due to Latex Mislabeling

    Cardinal Health is recalling ChemoPlus Protective Wrap-around Goggles because the kit labels state they are latex-free, but the goggle straps contain natural rubber latex.

    Product
    ChemoPlus Protective Wrap-around Goggles Product Code:DP5030G Product Usage: ChemoPlus chemotherapy spill kits are for the clean-up and containment of chemotherapy spills
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1286-2019·2019-05-15

    Cardinal Health Recalls ChemoPlus Chemo Spill Kits Due to Latex

    Cardinal Health 200, LLC is recalling ChemoPlus Chemo Spill Kits because the safety goggles inside contain natural rubber latex, despite the kit label stating the product is latex-free.

    Product
    ChemoPlus Chemo Spill Kit, Home Health Kit Product Code:DP5108K Product Usage: ChemoPlus chemotherapy spill kits are for the clean-up and containment of chemotherapy spills
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0354-2019·2018-12-26

    Enovachem Recalls Dyural-80 Injection Kits Due to Incorrect Latex Labeling

    Enovachem is recalling Dyural-80 Injection Kits because the product insert incorrectly stated that the stoppers do not contain latex, when they actually contain natural rubber latex.

    Product
    Dyural-80 Injection Kit, 1 Dose, Single Use Only, Rx only, Distributed by Enovachem Pharmaceuticals, Torrance, CA 90501, NDC 76420-0755-01
    Category
    Drug
    Distribution
    0 states
  • HighFDA (Devices)·Z-2576-2018·2018-08-08

    Arrow International Recalls Percutaneous Sheath Introducer Kits Due to Latex Labeling Error

    Arrow International is recalling 60 units of Percutaneous Sheath Introducer Kits because the product contains dry natural rubber latex but is labeled as latex-free.

    Product
    Percutaneous Sheath Introducer Kit for use with 7 - 7.5 Fr. Catheters (8 Fr. 10 cm sheath length .035 inch dia. spring-wire guide), REF ES-09807. The percutaneous sheath introducer permits venous access and catheter introduction to the central circulation.
    Category
    Medical Device
    Distribution
    1 state
  • SevereFDA (Devices)·Z-2036-2018·2018-06-06

    Recall of Sterile Powdered Surgical Gloves Due to Banned Powder Content

    WRP Asia Pacific Sdn Bhd is recalling 201,000 pairs of AmerisourceBergen sterile surgical gloves because some left-handed gloves contain powder, which is banned in the U.S.

    Product
    AmerisourceBergen PF Latex SG (Surgical Glove), Sterile, Powder Free, Size 6.5, Item No. 10112
    Category
    Medical Device
    Distribution
    9 states
  • HighFDA (Devices)·Z-1367-2018·2018-04-18

    Teleflex Medical Recalls Latex Rebreathing Bags Due to Missing Allergen Warning

    Teleflex Medical Europe Ltd is recalling 107,962 latex rebreathing bags because they lack the required warning that the product contains natural rubber latex, which may cause allergic reactions.

    Product
    Latex Rebreathing Bags: Product Code Equivalent Code (a) 151174050 151174 (b) 153000005 153000005 (c) 153000010 153000010 (d) 153000020 153000020 (e) 153000030 153000030 (f) 153000050 153000050 (g) 210700050 2107050 (h) 210700102 2107102 (I) 210700202 2107202 (j) 21070
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1370-2018·2018-04-18

    Teleflex Baker Jejunostomy Tubes Recalled for Missing Latex Warning

    Teleflex Medical Europe Ltd is recalling 200 Baker Jejunostomy Tubes because the packaging lacks a required warning that the product contains natural rubber latex.

    Product
    Baker Jejunostomy Tubes: Product Code Equivalent Code (a) 655300160 655316 (b) 655500200 655520
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1368-2018·2018-04-18

    Teleflex Medical Recalls Rectal Catheters Due to Missing Latex Warning

    Teleflex Medical Europe Ltd is recalling 6,340 rectal catheters because the packaging lacks a required warning that the product contains natural rubber latex.

    Product
    Rectal Catheters; Product Code Equivalent Code 580114 580114 Product Usage: Rectal Balloon Catheter is inserted into the rectum to measure the abdominal pressure as bladder filled.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1369-2018·2018-04-18

    Teleflex Recalls Simplastic Suprapubic Puncture Instruments for Missing Latex Warning

    Teleflex Medical Europe Ltd is recalling Simplastic Suprapubic Puncture Instruments because the packaging lacks a required warning that the products contain natural rubber latex.

    Product
    Simplastic Suprapubic Puncture Instruments: Product Code Equivalent Code (a) 650704100 551310 (b) 650704120 551312 (c) 650704160 551316 Product Usage: RUSCH Simplastic Suprapubic Puncture Instruments are indicated for emergency suprapubic drain
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1204-2018·2018-04-04

    Johnson & Johnson Recalls Select First Aid Wraps Due to Latex Labeling Error

    Johnson & Johnson is voluntarily recalling select first aid wraps because the label incorrectly states they are not made with natural rubber latex.

    Product
    Johnson & Johnson BAND-AID¿ Brand First Aid Products SECURE-FLEX¿ Wrap (size: 3in)
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-1202-2018·2018-04-04

    Johnson & Johnson Recalls COACH Self-Adhering Sports Wraps for Latex Labeling Error

    Johnson & Johnson is recalling COACH Self-Adhering Sports Wraps because the label incorrectly states they are not made with natural rubber latex, though latex was used in early manufacturing.

    Product
    COACH¿ Self-Adhering Sports Wrap (size: 3in)
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-1205-2018·2018-04-04

    Johnson & Johnson Recalls First Aid Wraps Due to Latex Labeling Error

    Johnson & Johnson is voluntarily recalling select first aid wraps because the 'not made with natural rubber latex' label is inaccurate.

    Product
    Johnson & Johnson BAND-AID¿ Brand First Aid Products HURT-FREE¿ Wrap (size: 1in)
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-1206-2018·2018-04-04

    Johnson & Johnson Recalls First Aid Wraps Due to Latex Labeling Error

    Johnson & Johnson is voluntarily recalling select first aid wraps because the packaging incorrectly states they are not made with natural rubber latex.

    Product
    Johnson & Johnson BAND-AID¿ Brand First Aid Products HURT-FREE¿ Wrap (size: 2in)
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-1203-2018·2018-04-04

    Johnson & Johnson Recalls First Aid Wraps Due to Latex Labeling Error

    Johnson & Johnson is recalling select first aid wraps because they were labeled as latex-free but used natural latex in early manufacturing.

    Product
    Johnson & Johnson BAND-AID¿ Brand First Aid Products SECURE-FLEX¿ Wrap (size: 2in)
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0946-2018·2018-03-21

    3M Recalls Ankle Braces Due to Missing Latex Warning Label

    3M is recalling specific ACE and Futuro ankle braces because they contain natural latex rubber but lack the required caution statement.

    Product
    ACE (TM) BRAND, DELUXE ANKLE BRACE, 207736, UPC 0 51131 20387 7
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-0945-2018·2018-03-21

    3M Recalls Futuro and ACE Ankle Supports Due to Missing Latex Warning

    3M is recalling Futuro and ACE ankle supports because they contain natural latex rubber but lack the required caution statement.

    Product
    FUTURO (TM) SPORT, QUICK STRAP ANKLE SUPPORT, REF 47736GEN, UPC 0 51131 19692 6
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Drugs)·D-0800-2017·2017-05-31

    Advanced Pharma Recalls Ofirmev Injection Due to Latex Labeling

    Advanced Pharma Inc. is recalling Ofirmev (Acetaminophen) injection because the product may contain synthetic or natural latex, which is not currently classified in the labeling.

    Product
    Ofirmev (Acetaminophen) injection all strengths, all dosage forms and all packaging, Rx Only, Avella of Houston, Houston, TX 77054
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0847-2017·2017-05-31

    Advanced Pharma Recalls Cardioplegic Solution for Latex Labeling Defect

    Advanced Pharma Inc. is recalling Cardioplegic Solution Maintenance due to a labeling error regarding potential latex content.

    Product
    Cardioplegic Solution Maintenance all strengths, all dosage forms and all packaging, Rx Only, Avella of Houston, Houston, TX 77054
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0849-2017·2017-05-31

    Advanced Pharma Recalls Potassium Phosphate Due to Latex Labeling Defect

    Advanced Pharma Inc. is recalling all strengths and dosage forms of Potassium Phosphate because the product may contain latex but lacks proper labeling.

    Product
    Potassium Phosphate all strengths, all dosage forms and all packaging, Rx Only, Avella of Houston, Houston, TX 77054
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0796-2017·2017-05-31

    Advanced Pharma Recalls Lidocaine Products Due to Latex Labeling Defect

    Advanced Pharma Inc. is recalling all Lidocaine products because they may contain latex but lack appropriate labeling.

    Product
    Lidocaine all strengths, all dosage forms and all packaging, Rx Only, Avella of Houston, Houston, TX 77054
    Category
    Drug
    Distribution
    Distributed nationwide