The Recall Desk

Hazard

Cut Injury recalls

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

What the numbers show

Total
61
Critical
1
Severe
9
Most recent
2024-10-31

Of the 61 cut injury recalls we have scored against our rubric, 1 (2%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 9 (15%) 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 cut injury 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 61

  • HighCPSC·25025·2024-10-31

    HALO Tumblers with Metal Straws Recalled for Laceration Hazard

    HALO Branded Solutions is recalling about 60,000 reusable tumblers with metal straws sold at Wawa stores due to a laceration hazard. The metal straw can cut the mouth and fingers; four injuries have been reported.

    Product
    Tumblers with a Metal Straw
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1482-2024·2024-07-24

    Primal Kitchen Avocado Oil Recalled for Glass Bottle Breakage Risk

    Kraft Heinz Foods Company is recalling Primal Kitchen Avocado Oil in 750ml glass bottles due to potential glass breakage. Affected bottles have Best When Used By dates of August 19-21, 2025.

    Product
    Primal Kitchen Avocado Oil 1PT 9.3 FL OZ (750ml) glass bottle UPC 855232007194, 6 bottles per wholesale case
    Category
    Food
    Distribution
    10 states
  • HighFDA (Devices)·Z-0105-2024·2023-10-18

    Multichem IA Plus and Controls Recalled Due to Broken Glass Vials

    TECHNO-PATH MANUFACTURING LTD. is recalling Multichem IA Plus and related controls due to broken glass vials that may expose laboratory personnel to biohazardous material. Affected lots should be discontinued immediately.

    Product
    Multichem IA Plus, Part Codes: a) 08P86-10, b) 08P86-19
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateNHTSA·22V883000·2022-11-29

    Winnebago Travel Trailers Recalled for Sharp Cabinet Door Handles

    Winnebago is recalling certain 2021-2022 travel trailers because cabinet door and drawer handles may have sharp edges. Dealers will replace the handles free of charge.

    Product
    WINNEBAGO — WINNEBAGO HIKE, MINNIE, MICRO MINNIE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0062-2022·2021-10-27

    Mountain Trail Mix recalled due to glass contamination

    Suntree Snack Foods is recalling Mountain Trail Mix 44 oz. packages because a customer reported finding glass pieces in the product.

    Product
    Mountain Trail Mix, 44 oz. containing 22 packs , UPC 814314024153 (inner unit), 814314024160 (outer unit). 4 master bags/case.
    Category
    Food
    Distribution
    12 states
  • SevereFDA (Food)·F-0209-2020·2019-12-11

    Hummingbird Wholesale Organic Chia Seeds Recalled for Metal Contamination

    Honey Heaven Wholesale Inc is recalling Hummingbird Wholesale Organic Chia Seeds due to a metal bar found in the product. The metal bar had a jagged edge and loose flakes.

    Product
    Hummingbird Wholesale Organic Chia Seeds, SD120-5#, packaged in a clear plastic bag with a while label, net wt. 5 lbs. No UPC code.
    Category
    Food
    Distribution
    2 states
  • HighFDA (Devices)·Z-0365-2020·2019-11-20

    Cadence Science Pressure Control Glass Syringes Recalled for Breakage Risk

    Cadence Science is recalling 237 Pressure Control Glass Syringes because they may break during use, posing a potential injury risk to patients and healthcare workers.

    Product
    Cadence Science Pressure Control Glass Syringe, Part Nos. 5338 (GTIN #816329023381); 5339 (GTIN #816329023398); 5340 (GTIN #816329023404); 5341 (GTIN #816329023411); 5342 (GTIN #816329023428); 5343 (GTIN #816329023435) - Product Usage: General Hospital Use
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2479-2018·2018-07-25

    Hitachi Oasis MRI Systems Recalled for Exposed Belt Hazard

    Hitachi Medical Systems America Inc is recalling 264 Oasis MRI systems because an exposed stainless steel belt can cause finger cuts.

    Product
    Hitachi Oasis MRI system Product Usage: Hitachi MR system is an imaging device and is intended to provide the physician with physiological and clinical information, obtained non-invasively and without the use of ionizing radiation. The Oasis system produces transverse, corona
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0892-2018·2018-03-14

    Heartland Coca-Cola Recalls Sprite Zero Cans Due to Sharp Edges

    Heartland Coca-Cola Bottling Company is recalling Sprite Zero cans because sharp edges on the cans could cut consumers' mouths.

    Product
    Sprite Zero, Lemon-Lime Soda, Zero Calories, 12 oz (355 mL) cans, packed in 12 packs, Canned under the authority of the Coca-Cola Company, Atlanta, GA
    Category
    Food
    Distribution
    6 states
  • HighFDA (Food)·F-0898-2018·2018-03-14

    Heartland Coca-Cola Recalls Orange Fanta Cans Due to Sharp Edges

    Heartland Coca-Cola Bottling Company is recalling Orange Fanta cans because sharp edges on the cans could cause cuts to consumers' mouths.

    Product
    Orange Fanta, Orange soda, Naturally flavored, 12 oz (355 mL) cans, packed in 12 and 24 packs, Canned under the authority of the Coca-Cola Company, Atlanta, GA
    Category
    Food
    Distribution
    6 states
  • HighFDA (Food)·F-0893-2018·2018-03-14

    Heartland Coca-Cola Recalls Mello Yola Cans Due to Sharp Edges

    Heartland Coca-Cola Bottling Company is recalling Mello Yola citrus-flavored soda cans because sharp edges on the cans could cut consumers' mouths.

    Product
    Mello Yello, Citrus Flavored Soda, 12 oz (355 mL) cans, packed in 12 packs, Canned under the authority of the Coca-Cola Company, Atlanta, GA
    Category
    Food
    Distribution
    6 states
  • HighFDA (Food)·F-0894-2018·2018-03-14

    Heartland Coca-Cola Recalls Grape Fanta Cans Due to Sharp Edges

    Heartland Coca-Cola Bottling Company is recalling 766,271 cases of Grape Fanta 12 oz cans because sharp edges on the cans could cause cuts to consumers' mouths.

    Product
    Grape Fanta, Grape Flavored Soda, 12 oz (355 mL) cans, packed in 12 packs, Canned under the authority of the Coca-Cola Company, Atlanta, GA
    Category
    Food
    Distribution
    6 states
  • HighFDA (Food)·F-0906-2018·2018-03-14

    Dr Pepper Diet Cans Recalled Due to Sharp Edges

    Heartland Coca-Cola Bottling Company is recalling Dr Pepper Diet cans because sharp edges were observed, posing a risk of cuts to consumers' mouths.

    Product
    Dr Pepper Diet, 12 oz (355 mL) cans, packed in 12 and 24 packs, Canned under the authority of Dr Pepper Company, Plano, TX
    Category
    Food
    Distribution
    6 states
  • HighFDA (Food)·F-0904-2018·2018-03-14

    Fresca Citrus Soda Recalled Due to Sharp Can Edges

    Heartland Coca-Cola Bottling Company is recalling Fresca Original Citrus Sparkling Flavored Soda cans because sharp edges were observed that could cause cuts to consumers' mouths.

    Product
    Fresca, Original Citrus Sparkling Flavored Soda, 12 oz (355 mL) cans, packed in 12 packs, Canned under the authority of the Coca-Cola Company, Atlanta, GA
    Category
    Food
    Distribution
    6 states
  • HighFDA (Food)·F-0905-2018·2018-03-14

    Heartland Coca-Cola Recalls Strawberry Fanta Cans Due to Sharp Edges

    Heartland Coca-Cola Bottling Company is recalling Strawberry Fanta cans because sharp edges were observed, posing a risk of cuts to consumers' mouths.

    Product
    Strawberry Fanta, Strawberry Flavored Soda, 12 oz (355 mL) cans, packed in 12 packs, Canned under the authority of the Coca-Cola Company, Atlanta, GA
    Category
    Food
    Distribution
    6 states
  • HighFDA (Food)·F-0896-2018·2018-03-14

    Heartland Coca-Cola Recalls Caffeine Free Coke Zero Cans Due to Sharp Edges

    Heartland Coca-Cola Bottling Company is recalling Caffeine Free Coke Zero cans because sharp edges were observed that could cause cuts to consumers' mouths.

    Product
    Caffeine Free Coke Zero, 12 oz (355 mL) cans, packed in 12 and 24 packs, Canned under the authority of the Coca-Cola Company, Atlanta, GA
    Category
    Food
    Distribution
    6 states
  • HighFDA (Devices)·Z-0504-2018·2018-02-07

    Beaver Optimum Safety Sideport Knife Recalled Due to Retracted Shield

    Beaver-Visitec is recalling 526,220 units of Optimum Safety Sideport Knives because the protective shield retracted, exposing the blade.

    Product
    bvi Beaver Optimum Safety Sideport Knife: (a) Straight 15o, REF 378235 (b) Straight 22.5o, REF 378236 (c) Straight 30o, REF 378237 (d) Straight 45o, REF 378238 Product Usage: Specialty blades and knives are used for stab and cut incisions in ophthalmic, ENT and other
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0502-2018·2018-02-07

    Beaver Xstar Safety Slit Knives Recalled Due to Retracted Protective Shield

    Beaver-Visitec International Inc. is recalling 659,370 units of bvi Beaver Xstar Safety Slit Knives because the protective shield was retracted, exposing the blade.

    Product
    bvi Beaver Xstar Safety Slit Knife: (a) REF 378214, 1.4mm, 45o Bevel Up (b) REF 378215, 1.50mm, 45o Bevel Up (c) REF 378217, 1.7mm, 45o Bevel Up (d) REF 378218, 1.8mm, 45o Bevel Up (e) REF 378220, 2.0mm, 45o Bevel Up (f) REF 378222, 2.2mm, 45o Bevel Up (g) REF 378223, 2
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0500-2018·2018-02-07

    Beaver-Visitec Recalls Safety Knives Due to Retracted Protective Shield

    Beaver-Visitec International Inc. is recalling specific EdgeAhead Safety Knives because the protective shield retracted, exposing the blade.

    Product
    bvi Beaver EdgeAhead Safety Knife, (a) Sideport MVR .90mm 20G, REF 370531 (b) Sideport Angled, .60mm (23G), REF 378233 Product Usage: Specialty blades and knives are used for stab and cut incisions in ophthalmic, ENT and other surgical applications.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0503-2018·2018-02-07

    Beaver Xstar Safety Crescent Blades Recalled Due to Exposed Blade

    Beaver-Visitec is recalling 123,240 units of Xstar Safety Crescent blades because the protective shield retracted, exposing the blade.

    Product
    bvi Beaver Xstar Safety Crescent, 2.5mm, 55o Bevel Up, REF 378234 Product Usage: Specialty blades and knives are used for stab and cut incisions in ophthalmic, ENT and other surgical applications.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0501-2018·2018-02-07

    Beaver Safety Sideport Knife Recalled Due to Retracted Protective Shield

    Beaver-Visitec International Inc. is recalling specific batches of Beaver Safety Sideport Knives because the protective shield retracted, exposing the blade.

    Product
    bvi Beaver Safety Sideport Knife: (a) 1.0mm, 45o, REF 378210 (b) 1.2mm, 45o, REF 378212 (c) 115mm, 45o, REF 378231 Product Usage: Specialty blades and knives are used for stab and cut incisions in ophthalmic, ENT and other surgical applications.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1576-2017·2017-03-15

    Stubb's Barbecue Sauce Recalled for Glass Bottle Defects

    McCormick & Co. is voluntarily recalling 18oz bottles of Stubb's Sticky Sweet BBQ Sauce due to glass defects that may cause chipped or missing glass.

    Product
    McCormick & Co., Inc., Stubbs Barbecue. 18oz Best By Date of January 17, 2020.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0110-2017·2016-11-02

    Roche Recalls cobas 6800/8800 Systems Due to Sharp Edge Injury Risk

    Roche is recalling 9,014 cobas 6800/8800 systems because a sharp edge on the sample rack tray caused four reported injuries.

    Product
    cobas 6800/8800 system Hepatitis Viral B DNA Detection Product Usage: The cobas p512 pre-analytical system is a computer controlled fully automatic system for sorting of open and closed barcoded and centrifuged sample tubes. It includes modules for registration and decapping
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0108-2017·2016-11-02

    Roche Recalls cobas p 471 Centrifuge Units Due to Sharp Edge Injury Risk

    Roche is recalling 9,014 cobas p 471 centrifuge units because a sharp edge on the sample rack tray caused four reported injuries.

    Product
    cobas p 471 centrifuge unit calculator/data processing module, for clinical use Product Usage: The cobas p312 pre-analytical system is a computer controlled stand-alone system for sorting and decapping sample tubes. As an option, the system works with an online connection.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0099-2017·2016-11-02

    Roche URISYS 2400 Urine Analyzer Recalled for Sharp Edge Injury Risk

    Roche is recalling URISYS 2400 Urine Analyzers because a sharp edge on the sample rack tray caused four reported injuries.

    Product
    URISYS 2400 Urine Analyzer Automated Urinalysis System Product Usage: The RSD 800 is a computer-controlled stand-alone sorting system for sorting barcoded samples. The system has an online connection to the host.
    Category
    Medical Device
    Distribution
    Distributed nationwide