The Recall Desk

Hazard

Packaging Defect recalls

1,604 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.

What the numbers show

Total
1,604
Critical
2
Severe
82
Most recent
2026-09-09

Of the 1,604 packaging defect recalls we have scored against our rubric, 2 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 82 (5%) 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 packaging defect 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.

1501–1525 of 1604

  • SevereFDA (Food)·F-0075-2014·2013-10-30

    Chobani Greek Yogurt Recalled Due to Illness Reports and Swollen Packaging

    Chobani is recalling specific lots of Greek yogurt due to reports of consumer illness and bloated packaging. Consumers should check their products for the affected dates.

    Product
    The Chobani Flip product come in 5.3oz (150g) square plastic containers with a foil lid. There are 12 containers per pack. Chobani 1.5% Milkfat Low-Fat Greek Yogurt Nutty for Nana-Flip, UPC 8-18290-01260-9
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0031-2014·2013-10-30

    Chobani Champions Greek Yogurt Recalled for Illness Reports and Swollen Packaging

    Chobani Champions Greek Yogurt is being recalled due to reports of consumer illness and bloated or swollen product packaging.

    Product
    Chobani Champions tubes, 2.25 oz., are sold in packages of 8, 16, or 36 counts per packages: 6/4/3.5 oz. Champions 1.5% Milkfat Low-Fat Greek Yogurt Blueberry, UPC 8-18290-01262-3; Chobani Champions also comes in 3.5 oz plastic cups: 8/8/2.25 oz. Champions 1.5% Milkfat L
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0012-2014·2013-10-30

    Chobani Greek Yogurt Recalled Due to Illness Reports and Swollen Packaging

    Chobani is recalling 0% Non-Fat Greek Yogurt Plain due to reports of illnesses and bloated, swollen product containers.

    Product
    12/6 oz. Chobani 0% Non-Fat Greek Yogurt Plain, UPC 8-94700-01001-4; 6/16 oz. Chobani 0% Non-Fat Greek Yogurt Plain, UPC 8-94700-01007-6; 6/32 oz. Chobani 0% Non-Fat Greek Yogurt Plain, UPC 8-94700-01013-7; 6/32 oz. Chobani 0% Non-Fat Greek Yogurt Plain-Club Pack, UPC 8-94700-
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0030-2014·2013-10-30

    Chobani Greek Yogurt Recalled Due to Illness Reports and Swollen Packaging

    Chobani is recalling specific lots of 0% Non-Fat Greek Yogurt Blueberry Fruit on the Bottom due to reported illnesses and bloated packaging.

    Product
    12/6 oz. Chobani 0% Non-Fat Greek Yogurt Blueberry Fruit on the Bottom, UPC 8-94700-01005-2; 6/6 oz. Chobani 0% Non-Fat Greek Yogurt Blueberry Fruit on the Bottom-6 Value Pack, UPC 8-94700-01041-0; 6/4/6 oz. Chobani 0% Non-Fat Greek Yogurt Blueberry Fruit on the Bottom-4 Value
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2315-2013·2013-10-09

    Atrium Medical Recalls Advanta VS Grafts Due to Label Adhesion

    Atrium Medical Corporation is recalling Advanta VS Grafts because the inner tray label may adhere to the outer tray, making it difficult to remove the tray onto the sterile field.

    Product
    Advanta VS Grafts >or= 6mm Intended for use in arterial vascular reconstruction, segmental bypass, and for arteriovenous vascular access.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2311-2013·2013-10-09

    Atrium Medical Recalls Advanta SST Grafts Due to Label Adhesion

    Atrium Medical Corporation is recalling Advanta SST Grafts because the inner tray label may adhere to the outer tray, making it difficult to remove the tray onto the sterile field.

    Product
    Advanta SST Grafts >or= 6mm Intended for use in arterial vascular reconstruction, segmental bypass, and for arteriovenous vascular access.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2317-2013·2013-10-09

    Atrium Medical Recalls Advanta SST Grafts Due to Label Adhesion

    Atrium Medical Corporation is recalling Advanta SST Grafts because the inner tray label may adhere to the outer tray, making removal difficult.

    Product
    Advanta SST Grafts <6mm Intended for use in arterial vascular reconstruction, segmental bypass, and for arteriovenous vascular access.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2314-2013·2013-10-09

    Atrium Flixene Grafts Recalled Due to Difficult Tray Removal

    Atrium Medical Corporation is recalling Flixene Trumpet Grafts because the inner tray label may adhere to the outer tray, making it difficult to remove the tray onto the sterile field.

    Product
    Flixene Trumpet Grafts >or= 6mm Flixene GW and GWT Grafts >or= 6mm Intended for use in arterial vascular reconstruction, segmental bypass, and for arteriovenous vascular access.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2309-2013·2013-10-09

    Atrium Medical Recalls Advanta VS Grafts Due to Label Adhesion Issue

    Atrium Medical Corporation is recalling Advanta VS Grafts because the inner tray label may adhere to the outer tray, making removal difficult.

    Product
    Advanta VS Grafts <6mm Intended for use in arterial vascular reconstruction, segmental bypass, and for arteriovenous vascular access.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2310-2013·2013-10-09

    Atrium Flixene Grafts Recalled Due to Difficult-to-Remove Inner Tray Label

    Atrium Medical Corporation is recalling Flixene Grafts because the inner tray label may adhere to the outer tray, making it difficult to remove the tray onto the sterile field.

    Product
    Flixene Grafts >or= 6mm Intended for use in arterial vascular reconstruction, segmental bypass, and for arteriovenous vascular access.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2306-2013·2013-10-09

    Atrium Medical Recalls Advanta SuperSoft Grafts Due to Label Adhesion

    Atrium Medical Corporation is recalling Advanta SuperSoft Grafts because the inner tray label may adhere to the outer tray, making it difficult to remove the tray onto the sterile field.

    Product
    Advanta SuperSoft Grafts >or= 6mm Intended for use in arterial vascular reconstruction, segmental bypass, and for arteriovenous vascular access.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2304-2013·2013-10-09

    Atrium Medical Recalls Advanta VXT Vascular Grafts Due to Label Adhesion

    Atrium Medical Corporation is recalling Advanta VXT Vascular Grafts because the inner tray label may adhere to the outer tray, making it difficult to remove the tray onto the sterile field.

    Product
    Advanta VXT Vascular Grafts >or= 6mm Intended for use in arterial vascular reconstruction, segmental bypass, and for arteriovenous vascular access.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2307-2013·2013-10-09

    Atrium Flixene IFG Recall Due to Label Adhesion Issue

    Atrium Medical Corporation is recalling Flixene IFG with Assisted Delivery because the inner tray label may adhere to the outer tray, making it difficult to remove the tray onto the sterile field.

    Product
    Flixene IFG with Assisted Delivery Intended for use in arterial vascular reconstruction, segmental bypass, and for arteriovenous vascular access.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2313-2013·2013-10-09

    Atrium Medical Recalls Advanta VXT Grafts Due to Label Adhesion Issue

    Atrium Medical Corporation is recalling Advanta VXT Grafts because the inner tray label may adhere to the outer tray, making it difficult to remove the tray onto the sterile field.

    Product
    Advanta VXT Grafts <6mm Intended for use in arterial vascular reconstruction, segmental bypass, and for arteriovenous vascular access.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2312-2013·2013-10-09

    Atrium Medical Recalls Advanta SuperSoft Grafts Due to Label Adhesion

    Atrium Medical Corporation is recalling Advanta SuperSoft Grafts because the inner tray label may adhere to the outer tray, making it difficult to remove the tray onto the sterile field.

    Product
    Advanta SuperSoft Grafts <6mm Intended for use in arterial vascular reconstruction, segmental bypass, and for arteriovenous vascular access.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2305-2013·2013-10-09

    Atrium Flixene IFG Vascular Grafts Recalled for Label Adhesion Issue

    Atrium Medical Corporation is recalling Flixene IFG Vascular Grafts because the inner tray label may adhere to the outer tray, making it difficult to remove the tray onto the sterile field.

    Product
    Flixene IFG Vascular Grafts >or= 6mm Intended for use in arterial vascular reconstruction, segmental bypass, and for arteriovenous vascular access.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2316-2013·2013-10-09

    Atrium Medical Recalls Advanta SST Grafts Due to Label Adhesion Issue

    Atrium Medical Corporation is recalling Advanta SST Grafts because the inner tray label may adhere to the outer tray, making it difficult to remove the tray onto the sterile field.

    Product
    Advanta SST Grafts <6mm Intended for use in arterial vascular reconstruction, segmental bypass, and for arteriovenous vascular access.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2260-2013·2013-09-25

    Integra Recalls Cranial Access Kits Due to Potential Sterile Seal Compromise

    Integra LifeSciences is recalling specific lots of Cranial Access Kits because the sterile package seal may become compromised during shipping.

    Product
    Cranial Access (CRAK) Kits, Product / Catalogue No.s: INSHITH, INSHITHND, INSHITHRZN The kits allow for access to the subarachnoid space or the lateral ventricles of the brain. The kits are intended to be used with an external drainage and monitoring system in selected patient
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1061-2013·2013-09-25

    Watson Recalls Hydrocodone and Acetaminophen Tablets Due to Defective Seals

    Watson Laboratories is recalling 875 bottles of Hydrocodone Bitartrate and Acetaminophen Tablets because defective bottles may have improperly seated tamper-evident seals.

    Product
    Hydrocodone Bitartrate and Acetaminophen Tablets, 7.5 mg/650 mg Tablets, 500 Count Bottle, Manufactured by: Watson Laboratories, Inc, Cocona, CA 92880, NDC 0591-2611-05.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2190-2013·2013-09-18

    HemoCue Glucose 201 Microcuvettes Recalled for Punctured Packaging

    HemoCue AB is recalling HemoCue Glucose 201 Microcuvettes because some single-pack pouches were found to be punctured during a complaint investigation.

    Product
    HemoCue¿ Glucose 201 Microcuvettes, 25 Microcuvettes Individually Packaged. The HemoCue Glucose 201 Microcuvettes are designed for use with the HemoCue Glucose 201 Analyzer and the HemoCue Glucose 201 DM Analyzer. Quantitative determination of glucose in whole blood using a
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-926-2013·2013-09-04

    Hospira Recalls Ketorolac Tromethamine Injections Due to Sterility Concerns

    Hospira, Inc. is recalling 345,800 vials of Ketorolac Tromethamine Injection due to a lack of assurance of sterility caused by loose or missing crimps on fliptop vials.

    Product
    KETOROLAC TROMETHAMINE — KETOROLAC TROMETHAMINE (KETOROLAC TROMETHAMINE)
    Category
    Drug
    Distribution
    0 states
  • ModerateFDA (Food)·F-1822-2013·2013-08-28

    Plum Organics Nutrition Blend Recalled for Ineffective Pouch Seals

    Plum Inc. is recalling Mighty 4 Essential nutrition blend pouches due to intermittent ineffective seals that may allow spoilage.

    Product
    Plum Organics Mighty 4 Essential nutrition blend; Purple Carrot Berry Quinoa, Greek yogurt in 4 oz pouch. Six pouches per box. USDA Organic. Selling case USPC: 846675003430; Case UPC: 00846675003553. Distributed by Plum Inc., Emeryville, CA.
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1823-2013·2013-08-28

    Plum Organics Nutrition Blend Recalled for Ineffective Pouch Seals

    Plum Inc. is recalling Mighty 4 Essential nutrition blend pouches due to intermittent ineffective hermetic seals that may allow spoilage after thermal processing.

    Product
    Plum Organics Mighty 4 Essential nutrition blend; Pumpkin Pomegranate Quinoa, Greek yogurt in 4 oz pouch. Six pouches per box. USDA Organic. Selling case UPC: 846675003454 Case USPC: 00846675003577 Distributed by Plum Inc., Emeryville, CA.
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1819-2013·2013-08-28

    Plum Organics Mighty 4 Nutrition Blend Recalled for Packaging Seal Defects

    Plum Inc. is recalling Mighty 4 Essential nutrition blend pouches due to intermittent ineffective hermetic seals that may allow spoilage.

    Product
    Plum Organics Mighty 4 Essential nutrition blend; Kale, Strawberry, Amaranth, Greek yogurt in 4 oz pouch. Six pouches per box. USDA Organic. Selling case USPC: 846675003409; Case USPC: 00846675003522 Distributed by Plum Inc., Emery ville, CA.
    Category
    Food
    Distribution
    Distributed nationwide