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.

826–850 of 1604

  • ModerateFDA (Devices)·Z-0214-2018·2017-12-20

    Terumo Recalls Glidesheath Introducer Sheaths Due to Packaging Seal Defect

    Terumo Medical Corp is recalling specific lots of Glidesheath Introducer Sheaths because an incomplete seal may compromise sterility.

    Product
    Glidesheath Slender Hydrophilic Coated Introducer Sheath, 5FR - 10CM (0.021), REF/Product Code RM*CS5F10NA, STERILE, Rx ONLY
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0217-2018·2017-12-20

    Terumo Recalls Glidesheath Introducer Sheaths Due to Packaging Seal Defect

    Terumo Medical Corp is recalling specific lots of Glidesheath Introducer Sheaths because an incomplete seal may compromise sterility.

    Product
    Glidesheath Slender Hydrophilic Coated Introducer Sheath A-Kit, 5FR - 10CM (0.021), REF/Product Code RM*ES5F10HAU, STERILE, Rx ONLY
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0229-2018·2017-12-20

    Terumo Recalls Glidesheath Introducer Sheaths Due to Packaging Seal Defect

    Terumo Medical Corp is recalling specific lots of Glidesheath Introducer Sheaths because an incomplete seal may compromise sterility.

    Product
    Glidesheath Slender Hydrophilic Coated Introducer Sheath, 7FR - 10CM (0.021), REF/Product Code RM*RS7F10PA, STERILE, Rx ONLY
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0222-2018·2017-12-20

    Terumo Recalls Glidesheath Introducer Sheaths Due to Packaging Seal Defect

    Terumo Medical Corp is recalling specific lots of Glidesheath Introducer Sheaths because an incomplete seal may compromise sterility.

    Product
    Glidesheath Slender Hydrophilic Coated Introducer Sheath A-Kit, 6FR - 10CM (0.025), REF/Product Code RM*ES6J10HAT, STERILE, Rx ONLY
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0221-2018·2017-12-20

    Terumo Recalls Glidesheath Introducer Sheaths Due to Packaging Seal Defect

    Terumo Medical Corp is recalling specific lots of Glidesheath Introducer Sheaths because an incomplete packaging seal may compromise sterility.

    Product
    Glidesheath Slender Hydrophilic Coated Introducer Sheath A-Kit, 6FR - 16CM (0.021), REF/Product Code RM*ES6F16HAU, STERILE, Rx ONLY
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0223-2018·2017-12-20

    Terumo Recalls Glidesheath Introducer Sheaths Due to Packaging Seal Defect

    Terumo Medical Corp is recalling specific lots of Glidesheath Introducer Sheaths because an incomplete seal may compromise sterility.

    Product
    Glidesheath Slender Hydrophilic Coated Introducer Sheath, 5FR - 10CM (0.021), REF/Product Code RM*RS5F10PA, STERILE, Rx ONLY
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0218-2018·2017-12-20

    Terumo Recalls Glidesheath Introducer Sheath Due to Incomplete Seal

    Terumo Medical Corp is recalling a specific lot of Glidesheath Introducer Sheaths because an incomplete seal may compromise sterility.

    Product
    Glidesheath Slender Hydrophilic Coated Introducer Sheath A-Kit, 5FR - 16CM (0.021), REF/Product Code RM*ES5F16HAU, STERILE, Rx ONLY
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0219-2018·2017-12-20

    Terumo Recalls Glidesheath Introducer Sheaths Due to Incomplete Packaging Seal

    Terumo Medical Corp is recalling specific lots of Glidesheath Introducer Sheaths because an incomplete seal may compromise sterility.

    Product
    Glidesheath Slender Hydrophilic Coated Introducer Sheath A-Kit, 5FR - 10CM (0.025), REF/Product Code RM*ES5J10HAT, STERILE, Rx ONLY
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0440-2018·2017-12-13

    JP's Delicacies Recalls Holi Aioli Lemon Basil Bottles

    JP's Delicacies LLC is recalling 1,344 bottles of Holi Aioli, Lemon Basil, 12oz, due to bulging bottles found during store inspections.

    Product
    Holi Aioli, Lemon Basil 12oz bottle
    Category
    Food
    Distribution
    6 states
  • ModerateFDA (Devices)·Z-0185-2018·2017-12-06

    Implant Direct Legacy Dental Implants Recalled for Packaging Defect

    Implant Direct Sybron Manufacturing is recalling 75 units of Legacy 3 Dental Implants because a packaging defect may compromise sterilization.

    Product
    ImplantDirect Legacy(TM) 3 Implant, 13MM L, REF 864713 This Legacy implant is a two-piece implant for one-stage or two-stage surgical procedures. These implants are intended for use in partially and fully edentulous upper and lower jaws in support of single or multiple-unit r
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0162-2018·2017-11-29

    Medline Recalls Sensicare Green Surgical Gloves Due to Potential Sterility Breach

    Medline Industries is recalling 8,000 units of Sensicare Green Surgical Gloves because a possible open seal on the packaging could compromise sterility.

    Product
    Sensicare Green Surgical Glove, PI, LF, PF. Packaged in a poly/poly peel pouch with Sunoco films, sterile. Surgical glove.
    Category
    Medical Device
    Distribution
    48 states
  • HighFDA (Devices)·Z-0065-2018·2017-11-15

    Encore Medical Recalls Cobalt MV Bone Cement Due to Packaging Seal Loss

    Encore Medical is recalling 840 units of Cobalt MV Bone Cement because the sterile Tyvek packaging seal may be lost, potentially compromising sterility.

    Product
    Cobalt MV Bone Cement 40GM, REF 402438, QTY 1, STERILE, Rx Only, Mfgr: BIOMET ORTHOPEDICS Cobalt MV and HV Bone Cement is indicated for use as bone cement in arthroplastic procedures of the hip, knee and other joints to fix plastic and metal prosthetic parts to living bone when
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0064-2018·2017-11-15

    Biomet Cobalt HV Bone Cement Recalled for Packaging Seal Loss

    Encore Medical is recalling Biomet Cobalt HV Bone Cement because the sterile Tyvek packaging seal may be lost, potentially compromising sterility.

    Product
    Cobalt HV Bone Cement 40GM, REF 402282, QTY 1, STERILE, Rx Only, Mfgr: BIOMET ORTHOPEDICS Cobalt MV and HV Bone Cement is indicated for use as bone cement in arthroplastic procedures of the hip, knee and other joints to fix plastic and metal prosthetic parts to living bone when
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0124-2018·2017-11-15

    San Gennaro Recalls Green Chili Cilantro Polenta Due to Unapproved Ink

    San Gennaro Foods is recalling Green Chili Cilantro Organic Polenta because date coding ink was printed directly on the food contact surface, allowing contact with the product.

    Product
    Green Chili Cilantro Organic Polenta, Ancient Harvest brand, Pre-cooked ready-to-heat, 12/18oz packages, UPC# 6-59201-10204-6 Green Chili Cilantro Organic Polenta, Frieda's brand, Pre-cooked just heat & serve, 12/16oz packages, UPC# 0-37842-04158-8 Ingredients: Water, Org
    Category
    Food
    Distribution
    18 states
  • ModerateFDA (Food)·F-0120-2018·2017-11-15

    San Gennaro Foods Recalls Polenta Due to Non-Approved Ink Contact

    San Gennaro Foods is recalling multiple brands of polenta because date coding ink was printed directly on the food contact surface of the packaging.

    Product
    Traditional Organic Polenta, Ancient Harvest brand, Pre-cooked ready-to-heat, 12/18 oz packages UPC#6-59201-10201-5 Traditional Organic Polenta, Italissima brand, Ready to heat and serve, 12/24 oz packages UPC# 7-78518-00760-5 Traditional Organic Polenta, Frieda's brand, P
    Category
    Food
    Distribution
    18 states
  • ModerateFDA (Food)·F-0127-2018·2017-11-15

    San Gennaro Polenta Recalled for Unapproved Ink on Food Contact Surface

    San Gennaro Foods is recalling pre-cooked polenta because date coding ink was printed directly on the food contact surface of the packaging.

    Product
    Traditional Polenta, San Gennaro brand, Pre-cooked Ready to Heat & Serve, 12/18 oz packages, UPC# 7-62676-15000-6 Traditional Polenta, San Gennaro brand, Pre-cooked Ready to Heat & Serve, 6/18oz packages, UPC# 7-62676-15000-6 Traditional Polenta, San Gennaro brand, Pre-coo
    Category
    Food
    Distribution
    18 states
  • ModerateFDA (Devices)·Z-0066-2018·2017-11-15

    Encore Medical Recalls Cobalt Bone Cement Due to Packaging Seal Loss

    Encore Medical, Lp is recalling 1,815 units of Cobalt MV with Gentamicin bone cement because the sterile Tyvek packaging seal was lost.

    Product
    Cobalt MV with Gentamicin, Cobalt Bone Cement 40GM, REF 402439, QTY 1, STERILE, Rx Only, Mfgr: BIOMET ORTHOPEDICS Cobalt MV and HV Bone Cement is indicated for use as bone cement in arthroplastic procedures of the hip, knee and other joints to fix plastic and metal prosthetic pa
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0129-2018·2017-11-15

    San Gennaro Sundried Tomato Polenta Recalled for Unapproved Packaging Ink

    San Gennaro Foods is recalling Sundried Tomato Polenta because date coding ink was printed directly on the food contact surface of the packaging.

    Product
    Sundried Tomato Polenta, San Gennaro brand, Pre-cooked Ready to Heat & Serve, 12/24 oz packages, UPC# 7-62676-12401-4 Sundried Tomato Polenta, San Gennaro brand, Pre-cooked Ready to Heat & Serve, 12/18 oz packages, UPC# 7-62676-15001-3 Sundried Tomato Polenta, San Gennaro C
    Category
    Food
    Distribution
    18 states
  • LowFDA (Food)·F-0122-2018·2017-11-15

    Frieda's Mushroom and Onion Organic Polenta Recalled for Unapproved Ink

    San Gennaro Foods is recalling Frieda's Mushroom and Onion Organic Polenta because date coding ink was printed directly on the food contact surface. The ink is not approved for food use.

    Product
    Mushroom and Onion Organic Polenta, Frieda's brand, Pre-cooked just heat & serve, 12/16oz packages, UPC# 0-37842-04155-7 Ingredients: Water, Organic Yellow Corn Meal, Organic Dried Mushrooms (may contain one or more of the following: porcini, chanterelle, shitake, portobello,
    Category
    Food
    Distribution
    18 states
  • LowFDA (Food)·F-0117-2018·2017-11-15

    Melissa's Sun-Dried Tomato Polenta Recalled for Unapproved Ink Contact

    San Gennaro Foods is recalling Melissa's Sun-Dried Tomato Polenta because date coding ink was printed on the food contact surface, allowing unapproved ink to contact the product.

    Product
    Sun-Dried Tomato Polenta, Melissa's brand, Shelf stable, 12/16 oz package UPC# 0-45255-11848-3 Ingredients: Water, Organic Cornmeal, Organic Sun-Dried Tomatoes, Organic Tomato Powder, Salt, Yeast Extract, Organic Granulated Onion, Tartaric Acid, Ascorbic Acid, Beta Carotene
    Category
    Food
    Distribution
    18 states
  • SevereFDA (Food)·F-3404-2017·2017-08-30

    Bush's Best Country Style Sauce Recalled for Defective Cans

    Bush Brothers & Co is recalling 28-ounce cans of Country Style Thick, Rich Sauce with Bacon & Extra Brown Sugar due to defective side seams that may allow C. botulinum growth.

    Product
    BUSHS BEST¿ Country Style THICK, RICH SAUCE WITH BACON & EXTRA BROWN SUGAR 28 OZ (1 LB 12 OZ) 794 g BUSH BROTHERS & COMPANY P. O. Box 52330, Dept, C KNOXVILLE, TN 37950-2330 UPC 0 39400 01974 9
    Category
    Food
    Distribution
    17 states
  • SevereFDA (Food)·F-3405-2017·2017-08-30

    Bush's Best Baked Beans Recalled for Defective Cans and Botulism Risk

    Bush Brothers & Co is recalling Bush's Best Baked Beans due to defective side seams that may allow C. botulinum growth.

    Product
    BUSHS BEST¿ Original SEASONED WITH BACON & BROWN SUGAR BAKED BEANS 28 OZ (1 LB 12 OZ) 794 g BUSH BROTHERS & COMPANY P. O. Box 52330, Dept, C KNOXVILLE, TN 37950-2330 UPC 0 39400 01614 4
    Category
    Food
    Distribution
    17 states
  • SevereFDA (Food)·F-3403-2017·2017-08-30

    Bush's Best Baked Beans Recalled for Defective Cans and Botulism Risk

    Bush Brothers & Co is recalling Bush's Best Brown Sugar Hickory Baked Beans due to defective side seams that may allow C. botulinum growth.

    Product
    BUSH'S BEST¿ Brown Sugar Hickory SWEET HICKORY SAUCE WITH BROWN SUGAR & SPICES BAKED BEANS 28 OZ (1 LB 12 OZ) 794 g BUSH BROTHERS & COMPANY P. O. Box 52330, Dept, C KNOXVILLE, TN 37950-2330 UPC 0 39400 01977 0
    Category
    Food
    Distribution
    17 states
  • ModerateFDA (Devices)·Z-3030-2017·2017-08-23

    CareFusion Recalls VersaSafe Plastic Cannulas Due to Packaging Punctures

    CareFusion 303, Inc. is recalling 1,546,800 units of VersaSafe Plastic Cannulas because punctures were detected in the blister packaging during the manufacturing process.

    Product
    VersaSafe Plastic Cannula - 11 Gauge, Model 9391-0200 Product Usage: Used with secondary IV sets or syringes with a female luer lock adapter to administer fluid and medications through a needle or catheter inserted into a patients artery or vein.
    Category
    Medical Device
    Distribution
    8 states
  • ModerateFDA (Drugs)·D-1051-2017·2017-08-09

    Bayer Recalls Alka-Seltzer Gold Tablets Due to Defective Blister Pack Foil

    Bayer HealthCare is recalling Alka-Seltzer Gold effervescent tablets because customer complaints confirmed small holes or cracks in the foil of the blister packs.

    Product
    Alka-Seltzer Gold (1000 mg Anhydrous citric acid, 344 mg Antacid Potassium bicarbonate, 1050 mg Antacid Sodium bicarbonate/Antacid) Effervescent Tablets, 36-count carton, Made in Germany, Distributed by Bayer HealthCare, LLC Whippany, NJ 07981, UPC 016500041085
    Category
    Drug
    Distribution
    Distributed nationwide