The Recall Desk

Severity 2 of 5

Moderate recalls

Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.

What “moderate” means here

Severity 2 (Moderate) recalls cover minor labeling errors, low-risk contamination, and voluntary precautionary recalls. The agency's own classification is typically FDA Class III, or the issue is something like incomplete instructions or a small UPC mismatch where the product itself is safe but doesn't meet documentation requirements. Use the same brand-name product safely; follow the manufacturer's instructions for return or exchange if you want a refund.

The full rubric is on the methodology page. Severity is computed deterministically from the agency’s own classification plus the source text — no editorial vibes.

7301–7325 of 21595

  • ModerateFDA (Food)·F-0830-2020·2020-03-18

    Kaiser Mild Banana Pepper Rings Recalled for Possible Foreign Material

    Kaiser Pickles LLC is recalling Mild Banana Pepper Rings due to possible foreign material. The product was distributed to 11 states.

    Product
    Kaiser Mild Banana Pepper Rings 1/4 KK in 1 gallon plastic bottles (4 gallons per case).
    Category
    Food
    Distribution
    11 states
  • ModerateFDA (Food)·F-0826-2020·2020-03-18

    Siete Grain Free Tortillas Recalled for Sodium Labeling Error

    Garza Food Ventures is recalling Siete Grain Free Burrito Size Tortillas because the sodium content is 340 mg per serving, not the 15 mg declared on the label.

    Product
    Siete Grain Free Burrito Size Tortillas Net Wt 15 oz (423g) 6 count UPC 865336000083 packaged in flexible plastic
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1006-2020·2020-03-18

    Redline Pharmacy Recalls Acetylcysteine Ophthalmic Solution Due to Processing Controls

    Redline Pharmacy Solutions is recalling Acetylcysteine Ophthalmic 10% Solution due to a lack of processing controls. The product was sold to patients in Nebraska.

    Product
    Acetylcysteine Ophthalmic 10% Solution, 5 mL per dropper bottle (10ML). Redline Specialty Pharmacy, 2415 Osborne Drive E, #100 Hastings, NE 68901
    Category
    Drug
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-1460-2020·2020-03-18

    Braemar DL950 Holter Monitor Recall Due to Startup Error

    Braemar Manufacturing is recalling DL950 Holter Monitors because a software issue prevents new patient studies from starting.

    Product
    Braemar Manufacturing LLC DL950 Holter Monitor 1285 Corporate Center Dr. Suite 150 Eagan, MN 55121 USA Rx Only
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0998-2020·2020-03-18

    Mayne Pharma Recalls Carbidopa and Levodopa Tablets Due to Foreign Tablet Mix-Up

    Mayne Pharma is recalling specific bottles of Carbidopa and Levodopa Tablets because a foreign tablet was found in a bottle.

    Product
    Carbidopa and Levodopa Tablets, USP 25 mg/250mg, 100 ct bottle, Rx Only, Mayne Pharma, Greenville, NC 27834. NDC 51862-858-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1471-2020·2020-03-18

    Verathon Recalls GlideScope Video Laryngoscope Operations and Maintenance Manuals

    Verathon, Inc. is recalling 239 GlideScope Video Laryngoscope Operations & Maintenance Manuals due to a typographical error regarding disinfection instructions.

    Product
    GlideScope Video Laryngoscope, Operations & Maintenance Manual, 0900-4940 REV 03
    Category
    Medical Device
    Distribution
    33 states
  • ModerateFDA (Drugs)·D-1056-2020·2020-03-18

    Lupin Recalls Levonorgestrel and Ethinyl Estradiol Tablets for Content Uniformity

    Lupin Pharmaceuticals is recalling specific lots of oral contraceptive tablets due to failed content uniformity tests.

    Product
    Levonorgestrel and Ethinyl Estradiol Tablets USP, 0.05mg/0.03 mg, 0.075mg/0.04mg, and 0.125mg/0.03mg, packaged in 1 Wallet of 28 Tablets (NDC 68180-857-11), 3 Wallets of 28 Tablets Each per carton (NDC 68180-857-13); Rx Only, Distributed by: Lupin Pharmaceuticals, Inc., Baltimore
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1438-2020·2020-03-11

    Polymer Technology Systems Recalls PTS Detect Cotinine In Vitro Diagnostic

    Polymer Technology Systems is recalling PTS Detect Cotinine in vitro diagnostic devices due to a lack of FDA 510(k) clearance.

    Product
    PTS Detect Cotinine, Ref. No. 3061, UPC 381933061017 in vitro diagnostic - Product Usage: The PTS Detect cotinine system provides quantitative measurement of the nicotine metabolite cotinine (25 200 ng/mL) in capillary (fingerstick) or venous whole blood. The test is for professi
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0776-2020·2020-03-11

    Natural Grocers Organic Extra Virgin Coconut Oil Recalled for Mold

    Vitamin Cottage Natural Food Markets is recalling 5,220 jars of Natural Grocers Organic Extra Virgin Coconut Oil because the product tested high for mold.

    Product
    Natural Grocers Organic Extra Virgin Coconut Oil, packaged in glass jars with metal lids and a plastic shrink seal, 32 oz. (946 mL), UPC# 849327-000375, Vitamin Cottage Natural Foods Markets (dba Natural Grocers) Lakewood, CO 80228. 12 units (jars)/case in cardboard box.
    Category
    Food
    Distribution
    20 states
  • ModerateFDA (Devices)·Z-1420-2020·2020-03-11

    Tosoh AIA-360 Analyzer Recalled Due to Display Screen Software Freeze

    Tosoh Bioscience Inc is recalling 12 AIA-360 Automated Immunoassay Analyzers because a software issue causes the display to freeze and stop the instrument.

    Product
    AIA-360 Automated Immunoassay Analyzer, Product Code 019945
    Category
    Medical Device
    Distribution
    5 states
  • ModerateFDA (Devices)·Z-1435-2020·2020-03-11

    Siemens Atellica IM Humidity Pack Recall Due to Software Error

    Siemens Healthcare Diagnostics is recalling Atellica IM Humidity Packs because a software error causes the analyzer to incorrectly eject them as expired.

    Product
    Atellica IM Humidity Pack (Qty 5), SMN 11313505, UDI 00630414234526, Software Version V1.21.0 and lower - Product Usage: The system is intended for the qualitative and quantitative analysis of various body fluids, using photometric, turbidimetric, chemiluminescent, and integrated
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1433-2020·2020-03-11

    Bard Biopsy EnCor Probe Recall for Performance Failures

    Bard Peripheral Vascular Inc is recalling specific Bard Biopsy EnCor Probes due to leaks, suction issues, and failure to obtain samples.

    Product
    Bard Biopsy EnCor Probe, MRI, 10G Trocar Tip, REF number ECPMR0110G, packaged individually in sterile pouches, 5 pouches/carton, Single Use, Rx, Sterile.
    Category
    Medical Device
    Distribution
    30 states
  • ModerateFDA (Devices)·Z-1434-2020·2020-03-11

    Bard Biopsy EnCor Probe Recall for Performance Failures

    Bard Peripheral Vascular Inc is recalling specific lots of Bard Biopsy EnCor Probes due to leaks, suction issues, and failure to obtain samples.

    Product
    Bard Biopsy EnCor Probe, MRI, 10G Blunt Tip, REF number ECPMR0110GBT, packaged individually in sterile pouches, 5 pouches/carton, Single Use, Rx, Sterile.
    Category
    Medical Device
    Distribution
    30 states
  • ModerateFDA (Food)·F-0775-2020·2020-03-11

    Natural Grocers Organic Extra Virgin Coconut Oil Recalled for Mold

    Vitamin Cottage Natural Food Markets is recalling Natural Grocers Organic Extra Virgin Coconut Oil because product tested high for mold.

    Product
    Natural Grocers Organic Extra Virgin Coconut Oil, packaged in glass jars with metal lids and a plastic shrink seal, 17.5 oz. (518 mL), UPC# 849327-000368, Vitamin Cottage Natural Foods Markets (dba Natural Grocers) Lakewood, CO 80228. 12 units (jars)/case in cardboard box.
    Category
    Food
    Distribution
    20 states
  • ModerateFDA (Devices)·Z-1408-2020·2020-03-11

    Medtronic Recalls McGRATH X3 Disposable Laryngoscope Blades Due to Fit Issues

    Medtronic is recalling McGRATH X3 Disposable Laryngoscope Blades because they may not fit the video laryngoscope handle or fit too tightly, potentially affecting optical performance.

    Product
    McGRATH X3 Disposable Laryngoscope Blades-used with the McGRATH MAC Video Laryngoscope to aid the intubation of the trachea Code: X3-002-000 (Individual Unit); X3-003-000 (Carton of 10 Units) - Product Usage: is a tool used to aid the intubation of the trachea. As a rigid lar
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0795-2020·2020-03-11

    Sticky Fingers Bakeries Gluten-Free Scones Recalled for Wheat Ingredient

    Custom Foods LLC is recalling Sticky Fingers Bakeries Gluten-Free Scones because wheat is listed in the ingredients, posing a risk to individuals with celiac disease or gluten sensitivity.

    Product
    Sticky Fingers Bakeries Gluten-Free Scones, Quick & Easy Mix, Meyer Lemon; Net Wt. 14 oz. (0.875 LBS) 396.9g. In Ingredient list: Lemon Flavored Pieces {sugar, enriched wheat flour (wheat flour, niacin, reduced iron Thiamin mononitrate, riboflavin, folic acid) Sticky Finger
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0774-2020·2020-03-11

    Driscoll's Raspberries Recalled for Pesticide Residue Exceeding Limits

    Driscoll's Inc. is recalling raspberries because in-house testing found Zeta-cypermethrin levels above the U.S. maximum residue limit.

    Product
    Driscoll's Raspberries- 6 oz. clamshell container 12 x 6 oz. per crate and 6 x 12 x 6 oz. (2 - 6 oz. attached clamshells) per crate UPC: 7 15756 10001 9 Product of Mexico
    Category
    Food
    Distribution
    10 states
  • ModerateFDA (Food)·F-0773-2020·2020-03-11

    Mothers' Milk Bank of Louisiana Recalls Donor Human Milk Bottles

    Mothers' Milk Bank of Louisiana at Ochsner Baptist is recalling 60 bottles of donor human milk due to a foreign object found in a bottle.

    Product
    Donor human milk in 3 oz. plastic bottles.
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Drugs)·D-0862-2020·2020-03-11

    Teva Recalls Mesalamine Tablets Due to Dissolution Test Failures

    Teva Pharmaceuticals USA is recalling 3,695 bottles of Mesalamine Delayed-Release Tablets because stability testing showed low dissolution results.

    Product
    MESALAMINE — MESALAMINE (MESALAMINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1436-2020·2020-03-11

    Siemens Atellica IM Humidity Pack Software Error Recall

    Siemens Healthcare Diagnostics is recalling Atellica IM Humidity Packs due to a software error that causes the analyzer to incorrectly eject them as expired.

    Product
    Atellica IM Humidity Pack (Qty 1), SMN 11313496, UDI 00630414243726, Software Version V1.21.0 and lower - Product Usage: Product Usage: The system is intended for the qualitative and quantitative analysis of various body fluids, using photometric, turbidimetric, chemiluminescent,
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0778-2020·2020-03-04

    Nature's Sunshine SmartMeal Shake Mix Recalled for Unapproved Herbicide in Flax Seed

    Pro-Form Manufacturing LLC is recalling Nature's Sunshine SmartMeal Nutritional Shake Mix because the flax seed used in the product contains an unapproved herbicide.

    Product
    Nature's Sunshine SmartMeal Nutritional Shake Mix; Natural Chocolate Flavor Net Wt. 1 lb. 3.5 oz. (555 Grams) UPC: 0 99904 03084 8 Product number: 6116 US3084 Distributed exclusively by: Nature's Sunshine Products, Inc. Spanish Fork, UT 84660
    Category
    Food
    Distribution
    2 states
  • ModerateFDA (Devices)·Z-1375-2020·2020-03-04

    Biomet 3i Recalls Bellatek Encode Healing Abutments Due to Rotation Error

    Biomet 3i is recalling specific Bellatek Encode Healing Abutments because they may cause incorrect rotation and margin misalignment in dental impressions.

    Product
    CERTAIN BELLATEK ENCODE HEALING ABUTMENT 4.1MM(D) X 5MM(P) X 3MM(H) Reference Number: IEHA453
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0746-2020·2020-03-04

    Domino Brown Sugar Recalled for Possible Foreign Material

    Domino Foods Inc is recalling 50 LB bags of Premium Pure Cane Medium Brown Sugar due to possible foreign material.

    Product
    Domino Premium Pure Cane Medium Brown Sugar, 50 LB bag, UPC 049200009727, Lots 50044 (Best By Jan 23, 2022) & 50045 (Best By Jan 24, 2022)
    Category
    Food
    Distribution
    23 states
  • ModerateFDA (Food)·F-0779-2020·2020-03-04

    Nature's Sunshine NutriSmart Vanilla Powder Recalled for Unapproved Herbicide

    Pro-Form Manufacturing LLC is recalling Nature's Sunshine NutriSmart Vanilla Powder because the flax seed ingredient contains an unapproved herbicide.

    Product
    Nature's Sunshine NutriSmart Polvo Para Preparar Bebida Sabor Vainilla Con In Toque Sabor a Chocolate; Vainilla Flavor Contenido Neto 510 g UPC: 0 99904 61532 8 Product number: 6116-MX61532 Importado y Distribuido por: Nature's Sunshine Products de Mexico, S.A. de C. V.
    Category
    Food
    Distribution
    2 states
  • ModerateFDA (Food)·F-0789-2020·2020-03-04

    Paleonola Grain Free Granola Recalled for Unapproved Herbicide Contamination

    Paleonola Llc is recalling Grain Free Granola and Maple Pancake products due to potential contamination with the unapproved herbicide haloxyfop.

    Product
    Paleonola Grain Free Granola; Maple Pancake; packaged in 10oz stand-up pouches; UPC 013964497120
    Category
    Food
    Distribution
    5 states