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Recall totals

All FDA and USDA recalls in Public Health Trace, June 2012 to September 2026.

37,115

Total recall recordsAll FDA and USDA recalls in Public Health Trace

9,793

Class I recallsReasonable probability of serious health consequences

24,343

Class II recallsTemporary or medically reversible health consequences

2,887

Class III recallsNot likely to cause adverse health consequences

Quick insights

A snapshot of the most notable patterns across all recorded FDA and USDA recalls.

Most recalled product100 vegetarian Fenugreek Capsules 90 count, 600mg, packaged in 150cc Amber Glass Packer with White Polypropylene Cap. 53 recalls

Most common hazardLack of Assurance of Sterility 2,072 recalls

Newest recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/so-delicious-dairy-freer-issues-voluntary-recall-salted-caramel-cluster-non-dairy-frozen-dessertPublished September 15, 2026

Most affected stateHawaii 200 recalls mention this state

State: AS ×
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Recalls announced by month (Year to date)

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Source: FDA and USDA public dataLast updated September 15, 2026 ET

Summary (Year to date)

1,527 recalls have been announced year to date.
Aug 2026 was 24% lower than the previous complete period (Jul 2026: 240).
The highest complete period was Jun 2026 (297).
Sep 2026 is incomplete and not included in the figures above.

Complete data
Incomplete

Recalls by class

Recalls by class
Class	Recalls
Class II	24,343
Class I	9,793
Class III	2,887
Not Yet Classified	1

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Recalls by class
Class	Recalls
Class II	24,343
Class I	9,793
Class III	2,887
Not Yet Classified	1

FDA Recall Terminated Historical recordClass II

ePHEDrine Sulfate 10 mg per mL 50 mg per 5 mL in 0.9% 5 mL Sodium Chloride 5 mL syringe, For IV Use, Rx Only, PharMEDium 913 N Davis Avenue Cleveland, MS NDC 71030-001-09

by PharMEDium Services, LLC

Reason: Firm is recalling 46 lots of various products because of a lack of sterility assurance.
Published: April 15, 2020
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

ePHEDrine Sulfate 5 mg per mL 25 mg per 5 mL, in 0.9% Sodium Chloride, 5 mL BD Syringe, For IV Use, Rx Only, PharMEDium 913 N. Davis Ave. Cleveland, MS 98732 NDC 71030-003-02

by PharMEDium Services, LLC

Reason: Firm is recalling 46 lots of various products because of a lack of sterility assurance.
Published: April 15, 2020
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

fentaNYL Citrate 50 mcg per mL, (Preservative Free) Injection, For IV use, 1,500 mcg per 30 mL, 30 mL Total Volume, in a 35 mL Monoject Barrel Syringe, PharMEDium Services, LLC 913 N. Davis Avenue Cleveland, MS 38732. NDC 61553-672-44

by PharMEDium Services, LLC

Reason: Firm is recalling 46 lots of various products because of a lack of sterility assurance.
Published: April 15, 2020
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

ePHEDrine Sulfate, 5 mg per mL, 25 mg per 5 mL in 0.9% Sodium Chloride, 5 mL syringe, For IV use, Preservative Free, PharMEDium 913 W Davis Ave Cleveland MS 38732 NDC 71030-003-09

by PharMEDium Services, LLC

Reason: Firm is recalling 46 lots of various products because of a lack of sterility assurance.
Published: April 15, 2020
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

rocuronium Bromide, 10 mg per mL, 50 mg per 5 mL, 5 mL BD Syringe, for IV Use, PharMEDium 13N. Davis Ave. Cleveland MS 36732. NDC 71019-321-05

by PharMEDium Services, LLC

Reason: Firm is recalling 46 lots of various products because of a lack of sterility assurance.
Published: April 15, 2020
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

succinylcholine Chloride, 20 mg per 5 mL, 100 mg per 5 mL, 5 mL BD Syringe, For IV Use, PharMEDium 913 N. Davis Ave, Cleveland, MS. NDC 71019-341-04

by PharMEDium Services, LLC

Reason: Firm is recalling 46 lots of various products because of a lack of sterility assurance.
Published: April 15, 2020
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

fentaNYL Citrate 10 mcg per mL, 2,500 mcg per 250 mL, 250 mL in a LifeCare Bag, in Sodium Chloride 0.9%. Rx Only, PharMEDium Services, LLC 913 N. Davis Ave Cleveland, MS 36732 NDC 61553-113-50

by PharMEDium Services, LLC

Reason: Firm is recalling 46 lots of various products because of a lack of sterility assurance.
Published: April 15, 2020
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

HYDROmorphone in 0.9% Sodium Chloride HCl, 1 mg per mL, For IV Use, 30 mg per 30 mL, 30 mL in a 35 mL Monoject Barrel Syringe, PharMEDium Services LLC 913 M. Davis Ave Cleveland, MS. NDC 61553-166-44

by PharMEDium Services, LLC

Reason: Firm is recalling 46 lots of various products because of a lack of sterility assurance.
Published: April 15, 2020
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

rocuronium Bromide 10 mg per mL 50 mg per 5 mL, 5 mL BD Syringe, For IV Use, PharMEDium 913 N. Davis Ave. Cleveland, MS. Preservative Free, NDC 71019-321-10

by PharMEDium Services, LLC

Reason: Firm is recalling 46 lots of various products because of a lack of sterility assurance.
Published: April 15, 2020
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

nICARdipine HCl (0.1 mg/mL) 1 mg/10mL, in 0.9% Sodium Chloride Injection USP, 10 ml in a 20mL syringe, Rx Only, PharMEDium Services LLC 12620 W. Airport Boulevard #130 Sugar Land, TX 77470. NDC 71019-206-01

by PharMEDium Services, LLC

Reason: Firm is recalling 46 lots of various products because of a lack of sterility assurance.
Published: April 15, 2020
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

ePHEDrine Sulfate, 5 mg per mL, 50 mg per 10 mL, In 0.9% Sodium Chloride 10 mL syringe, For IV Use Preservative Free PharMEDium 913 N. Davis Ave. Cleveland, MS NDC 71030-003-12

by PharMEDium Services, LLC

Reason: Firm is recalling 46 lots of various products because of a lack of sterility assurance.
Published: April 15, 2020
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Fentanyl Citrate Injection, USP, 100 mcg/2 mL (50 mcg/mL), 10 Ampules per carton, (2 mL each), Rx only, Manufactured by: Akorn, Inc., Lake Forest, IL 60045, NDC 17478-030-02

by Akorn Inc

Reason: Failed impurities/degradation specification: Out-of-Specification result for total impurity at 4.1% (Limit: NMT 3.0%) during retained sample testing.
Published: April 8, 2020
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass I

Phytonadione Injectable Emulsion, USP, 10 mg/mL 1 mL ampule (NDC 43598-405-11) packaged in 25 x 1 mL Single-Dose Ampules per carton (NDC 43598-405-16); Rx Only, Distributor: Dr. Reddy's Laboratories Inc., Princeton, NJ 08540.

by Dr. Reddy's Laboratories, Inc.

Reason: Defective Container: Recall is due to breaking and shattering of ampules upon opening
Published: April 8, 2020
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Lisinopril Tablets USP, 30 mg, 100-count bottle, Rx only, Manufactured for: Lupin Pharmaceuticals, Inc., Baltimore, Maryland 21202, NDC 68180-982-01

by Lupin Pharmaceuticals Inc.

Reason: Presence of Foreign Tablet/ Capsule: Product complaint received indicating mix-up of one lisinopril 5mg tablet inside of a 30 mg, 100-count bottle of Lisinopril Tablets.
Published: April 8, 2020
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

New Capstone, Inc

Product: ReStructure VANILLA PROTEIN POWDER NET WT. 527G POUCH & 27G…
Reason: The firm was notified that the labeling does not include the word milk on the ingredient statement
Published: April 8, 2020
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Nystatin Oral Suspension, USP, 100,000 units per mL, Cherry/Peppermint Flavor, 16 fl oz (473 mL) bottle, Rx ONLY, pai Pharmaceutical Associates, Inc., Greenville, SC 29605; NDC 0121-0810-16.

by PAI Holdings, LLC. dba Pharmaceutical Associates Inc

Reason: SubPotent Drug: Low out-of-specification results for assay testing.
Published: April 1, 2020
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Tacrolimus Capsules, USP 5mg, 100-count bottle, Rx only, Mylan Pharmaceuticals Inc., Morgantown, WV 26505, NDC 0378-2047-01

by Mylan Pharmaceuticals Inc.

Reason: Presence of foreign tablet/capsule - Potential presence of commingled one Tacrolimus 1 mg capsule in 5 mg bottles.
Published: April 1, 2020
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Colostat, Homeopathic Remedy, 1 fl. oz. (30 mL) per bottle, 20% Ethanol, Dist. by Energique, Inc., 201 Apple Blvd., Woodbine, IA 51579, NDC 44911-0411-1

by Grato Holdings, Inc.

Reason: Labeling mix-up - Indications on product label are incorrect.
Published: April 1, 2020
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass III

Organic By Nature, Inc.

Product: Touchstone Essentials Organic Super Protein Vanilla Coconut…
Reason: Firm was notified by supplier that Organic Ground Flaxseed powder was under recall by manufacturer due to unapproved herbicide - Haloxyfop
Published: April 1, 2020
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass III

Organic By Nature, Inc.

Product: Touchstone Essentials Super Greens Juice - Raspberry Apple;…
Reason: Firm was notified by supplier that Organic Ground Flaxseed powder was under recall by manufacturer due to unapproved herbicide - Haloxyfop
Published: April 1, 2020
Distribution: Nationwide

View recall →

Data last updated: September 15, 2026 ET

Recall records are summarized from official FDA and USDA sources. Notices may be updated, reclassified, terminated, or withdrawn. Always review the linked official notice for the most current instructions. Read the full medical disclaimer.