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.

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.

676–700 of 1604

  • ModerateFDA (Devices)·Z-1243-2019·2019-05-08

    Molnlycke Recalls EZ Derm Porcine Xenograft Due to Heat Seal Failures

    Molnlycke Health Care is recalling 1,332 units of EZ Derm Porcine Xenograft due to intermittent heat seal failures on the outer pouch.

    Product
    EZ Derm Porcine Xenograft, labeled as the following: a. EZ Derm 3x4 (8x10 cm) Non-Perforated, Part Number: 131703-03; b. EZ Derm 7 x 18 (17 x 46 cm) Non-Perforated, Part Number: 131704-03; c. EZ Derm 2 x 2 (5 x 5 cm) Non-Perforated, Part Number: 131705-03; d.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1319-2019·2019-05-08

    Harmless Harvest Recalls Dairy-Free Yogurt Drinks Due to Packaging Defect

    Harmless Harvest Inc. is voluntarily recalling specific lots of Dairy-Free Yogurt Drinks due to a packaging defect that may cause premature spoilage.

    Product
    Harmless Harvest Dairy-Free Yogurt Drink; Cultured Coconut Drink: Probiotic Blueberry. 8 fl. oz. plastic bottle; UPC 859078-002986
    Category
    Food
    Distribution
    4 states
  • ModerateFDA (Food)·F-1318-2019·2019-05-08

    Harmless Harvest Recalls Strawberry Coconut Drink Due to Packaging Defect

    Harmless Harvest is voluntarily recalling specific lots of its Strawberry Probiotic Coconut Drink due to a packaging defect that may cause premature spoilage.

    Product
    Harmless Harvest Dairy-Free Yogurt Drink; Cultured Coconut Drink - Probiotic Strawberry. 8 fl. oz. plastic bottle; UPC 859078-002979
    Category
    Food
    Distribution
    4 states
  • LowFDA (Devices)·Z-1198-2019·2019-04-24

    Cordis Guiding Catheters Recalled for Frayed Mounting Card Fragments

    Cordis Corporation is recalling Vista Brite Tip and Androit guiding catheters because frayed pieces of the mounting card were found inside the primary packaging.

    Product
    Cordis Vista Brite Tip & Androit Guiding Catheters Product Usage: The guiding catheter is intended for use for intravascular introduction of interventional/diagnostic devices into the coronary or peripheral vascular systems.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1132-2019·2019-04-24

    Estee Lauder Recalls Repairwear Cream Due to Ineffective Container Seal

    Estee Lauder Inc is recalling 14,490 jars of Repairwear Laser Focus Line Smoothing Cream SPF 15 because the seal between the cap and jar is ineffective.

    Product
    Repairwear Laser Focus Line Smoothing Cream Broad Spectrum SPF 15, packaged in a light green folding carton containing a 50 mL silver jar with a silver cap, Clinique Laboratories, Dist. New York, NY 10022
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1131-2019·2019-04-17

    ACUVUE OASYS for Astigmatism Contact Lenses Recalled for Packaging Seal Defects

    Johnson & Johnson Vision Care is recalling one lot of ACUVUE OASYS for Astigmatism contact lenses due to potential incomplete packaging seals.

    Product
    ACUVUE OASYS for ASTIGMATISM brand contact lenses, Base Curve 8.6 Refractive Power -1.00D, -1.25D x 100, 6 pack.
    Category
    Medical Device
    Distribution
    1 state
  • LowFDA (Drugs)·D-1058-2019·2019-04-03

    Ingenus Recalls Diclofenac Sodium Topical Solution Due to Leaking Bottles

    Ingenus Pharmaceuticals is recalling 29,435 bottles of Diclofenac Sodium Topical Solution because some bottles were found leaking.

    Product
    Diclofenac Sodium Topical Solution, 1.5% w/w, 5 FL. OZ. (150 mL) bottle, Rx Only, Manufactured for: Ingenus Pharmaceuticals, LLC, Orlando, FL 32839-6408, NDC 50742-308-05.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1157-2019·2019-03-20

    Kradjian Importing Recalls Zarrin Pickled Cucumbers Due to Leaking Cans

    Kradjian Importing Co is recalling Zarrin Pickled Cucumbers & Cornichons because some cans are leaking and swollen. Consumers should stop using the product.

    Product
    Zarrin Pickled Cucumbers & Cornichons: Net Weight 101.4 oz. 3 kg. Ingredients: Cucumber, water, salt, acid (acetic acid, spices, food coloring (tartrazine). Refrigerate after opening. UPC 7 64363 18305 2 Product of the West Bank Packed for Blanish International, PO Box 2
    Category
    Food
    Distribution
    14 states
  • ModerateFDA (Food)·F-1158-2019·2019-03-20

    Kradjian Imports Recalls Leaking and Swollen Bulgarian White Brined Sheep's Milk Cheese

    Kradjian Imports Co. is recalling 952 cases of Bulgarian White Brined Sheep's Milk cheese due to leaking and swollen cans. The product was distributed across 14 states.

    Product
    Bulgarian White Brined Sheep's Milk cheese; 5 gallon can Ingredients: Pasteurized Sheep's Milk, Bacterial culture, salt, rennet. Product of Belgium. Imported by Kradjian Imports Co., Inc., Glendale, CA 91204
    Category
    Food
    Distribution
    14 states
  • ModerateFDA (Drugs)·D-0992-2019·2019-03-13

    Apotex Recalls Out-of-Sequence Contraceptive Tablets

    Apotex Inc. is recalling specific lots of Drospirenone and Ethinyl Estradiol tablets because they may be missing or placed incorrectly in the blister pack.

    Product
    Drospirenone and Ethinyl Estradiol Tablets, USP, 3 mg/0.03 mg, 28 Tablets Blister, 1 Unit (NDC 60505-4183-1) packaged as 84 Tablets Blister, 3x1 Unit per carton (NDC 60505-4183-3), Rx Only, Manufactured for: Apotex Corp., Weston, FL 33326; Manufactured by: Oman Pharmaceutical Pr
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0219-2019·2018-11-14

    Orexigen Recalls Contrave Tablets Due to Container Packaging Defect

    Orexigen Therapeutics is recalling 18,895 bottles of Contrave extended-release tablets due to a container packaging defect. The affected lot is ZYCY with an expiration date of 04/11/2021.

    Product
    CONTRAVE — CONTRAVE (NALTREXONE HYDROCHLORIDE AND BUPROPION HYDROCHLORIDE)
    Category
    Drug
    Distribution
    0 states
  • HighFDA (Devices)·Z-0234-2019·2018-10-31

    Ecolab Recalls Da Vinci Robotic System Disposable Accessory Kits

    Ecolab is recalling specific lots of Disposable Accessory Kits for the Da Vinci Si Robotic system because wrinkles in the packaging seal could compromise sterility.

    Product
    Disposable Accessory Kit, 4-Arm (Box of 5) individually sealed in poly-Tyvek pouches / Rx Sterile / to used exclusively on the Intuitive Surgical Da Vinci Si Robotic system / Distributed by Intuitive Surgical Product Usage: Microtek Medical Equipment Drapes are intended to co
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0231-2019·2018-10-31

    Ecolab recalls sterile instrument arm drapes due to potential seal defects

    Ecolab is recalling specific lots of sterile instrument arm drapes for the Da Vinci Si system because seal wrinkles may compromise sterility.

    Product
    Instrument Arm Drape (Box of 20) individually sealed in poly-Tyvek pouches / Rx Sterile / to used exclusively on the Intuitive Surgical Da Vinci Si Robotic system Distribute by Intuitive Surgical Product Usage: Microtek Medical Equipment Drapes are intended to cover/wrap vari
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0233-2019·2018-10-31

    Ecolab Recalls Disposable Accessory Kits for Da Vinci Robotic System

    Ecolab Inc is recalling specific lots of Disposable Accessory Kits, 3-Arm, due to potential pouch seal defects that could compromise sterility.

    Product
    Disposable Accessory Kit, 3-Arm (Box of 5) individually sealed in poly-Tyvek pouches / Rx Sterile / to used exclusively on the Intuitive Surgical Da Vinci Si Robotic system / Distributed by Intuitive Surgical Product Usage: Microtek Medical Equipment Drapes are intended to co
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0149-2019·2018-10-24

    Zimmer Biomet Recalls Affixus Hip Fracture Nails Due to Packaging Defects

    Zimmer Biomet is recalling 30 Affixus Hip Fracture Nails because sterile packaging was found open during surgery, posing a risk of infection.

    Product
    Affixus Hip Fracture Nail Left 125 9 mm x 460 mm, Item Number 814409460 Product Usage: Intended for the fixation of fractures
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0159-2019·2018-10-24

    Zimmer Biomet Recalls Affixus Hip Fracture Nails Due to Packaging Defects

    Zimmer Biomet is recalling 39 Affixus Hip Fracture Nails because sterile packaging was found open during surgery.

    Product
    Affixus Hip Fracture Nail Right 130 11 mm x 320 mm, Item Number 814511320 Product Usage: Intended for the fixation of fractures
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0166-2019·2018-10-24

    Zimmer Biomet Recalls Affixus Hip Fracture Nails Due to Packaging Defects

    Zimmer Biomet is recalling 41 Affixus Hip Fracture Nails because sterile packaging was found open during surgery.

    Product
    Affixus Hip Fracture Nail Left 130 11 mm x 380 mm, Item Number 814611380 Product Usage: Intended for the fixation of fractures
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0140-2019·2018-10-24

    Zimmer Biomet Recalls Affixus Hip Fracture Nails Due to Packaging Defect

    Zimmer Biomet is recalling 22 Affixus Hip Fracture Nails because sterile packaging was found open during surgery.

    Product
    Affixus Hip Fracture Nail Right 125 13 mm x 280 mm, Item Number 814313280 Product Usage: Intended for the fixation of fractures
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0167-2019·2018-10-24

    Zimmer Biomet Recalls Affixus Hip Fracture Nails Due to Packaging Defect

    Zimmer Biomet is recalling 16 Affixus Hip Fracture Nails because sterile packaging was found open during surgery. The recall covers units distributed in the US and abroad.

    Product
    Affixus Hip Fracture Nail Left 130 11 mm x 400 mm, Item Number 814611400 Product Usage: Intended for the fixation of fractures
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0169-2019·2018-10-24

    Zimmer Biomet Recalls Affixus Hip Fracture Nails Due to Packaging Defect

    Zimmer Biomet is recalling 20 Affixus Hip Fracture Nails because sterile packaging was found open during surgery. The recall covers units distributed in the US and abroad.

    Product
    Affixus Hip Fracture Nail 125 9 mm x 165 mm, Item Number 816709165 Product Usage: Intended for the fixation of fractures
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0132-2019·2018-10-24

    Zimmer Biomet Recalls Affixus Hip Fracture Nails Due to Packaging Defects

    Zimmer Biomet is recalling 27 Affixus Hip Fracture Nails because sterile packaging was found open during surgery. The recall covers units distributed in the US and abroad.

    Product
    Affixus Hip Fracture Nail Right 125 11 mm x 340 mm, Item Number 814311340 Product Usage: Intended for the fixation of fractures
    Category
    Medical Device
    Distribution
    Distributed nationwide