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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: NC ×
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Recalls announced by month (Year to date)

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Source: FDA and USDA public dataLast updated September 17, 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

Clobetasol Propionate Ointment USP, 0.05%, packaged in a) 15 grams tube, NDC 52565-039-15; b) 30 grams tube, NDC 52565-039-30; c) 45 grams tube, NDC 52565-039-45; d) 60 grams tube, NDC 52565-039-60, Rx only, Manufactured by: Teligent Pharma, Inc., Buena, NJ 08310.

by Teligent Pharma, Inc.

Reason: cGMP deviations: all products within expiry are being recalled because the firm is discontinuing its stability study program.
Published: March 30, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Clobetasol Propionate Lotion, 0.05%, packaged in a) 2 fl. oz. (59 mL) bottles, NDC 52565-055-02; b) 4 fl. oz. (118 mL) bottles, NDC 52565-055-04, Rx Only, Manufactured by: Teligent Pharma, Inc., Buena, New Jersey 08310.

by Teligent Pharma, Inc.

Reason: cGMP deviations: all products within expiry are being recalled because the firm is discontinuing its stability study program.
Published: March 30, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Clobetasol Propionate Cream USP, 0.05% (Emollient), packaged in a) 15 grams tube, NDC 52565-094-15; b) 30 grams tube, NDC 52565-094-30; c) 45 grams tube, NDC 52565-094-45; d) 60 grams tube, NDC 52565-094-60, Rx only, Manufactured by: Teligent Pharma, Inc., Buena, NJ 08310.

by Teligent Pharma, Inc.

Reason: cGMP deviations: all products within expiry are being recalled because the firm is discontinuing its stability study program.
Published: March 30, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Clobetasol Propionate Cream USP, 0.05%, packaged in a) 15 grams tube, NDC 52565-051-15; b) 30 grams tube, NDC 52565-051-30; c) 45 grams tube, NDC 52565-051-45; d) 60 grams tube, NDC 52565-051-60; Rx only, Manufactured by: Teligent Pharma, Inc., Buena, NJ 08310.

by Teligent Pharma, Inc.

Reason: cGMP deviations: all products within expiry are being recalled because the firm is discontinuing its stability study program.
Published: March 30, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Betamethasone Dipropionate Lotion USP, 0.05%* (Augmented), packaged in a) 30 mL (29 grams) bottles, NDC 52565-023-29; b) 60 mL (58 grams) bottles, NDC 52565-023-59, Rx Only, Teligent Pharma, Inc., Buena, NJ 08310

by Teligent Pharma, Inc.

Reason: cGMP deviations: all products within expiry are being recalled because the firm is discontinuing its stability study program.
Published: March 30, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass I

REVITADERM WOUND CARE GEL, (Benzalkonium Chloride in a gel containing transforming growth factor-b), 0.1%, packaged in 29.6 mL (1.0 FL OZ) bottles (NDC 63347-120-02) and 88.7 mL (3.0 FL OZ) tubes (NDC 63347-120-01), Blaine Labs Inc., Santa Fe Springs, CA 90670

by Blaine Labs Inc

Reason: Microbial Contamination of Non-sterile Product; FDA analysis found the product to be contaminated with Bacillus cereus.
Published: March 30, 2022
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Schreiber Foods Inc

Product: Shredded Cheese consisting of Monterey Jack, Queso Quesadill…
Reason: Potential to contain foreign material (metal).
Published: March 30, 2022
Distribution: 3,720 cases distributed on 3/6/22 and 3/…

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FDA Recall Terminated Historical recordClass I

Avaphinal Maximum Male Enhancement Sexual Pills, 2000 MG*, packaged in 10 Capsules per carton.

by Walmart Stores

Reason: Marketed Without An Approved NDA/ANDA: Product was found to contain undeclared sildenafil, an ingredient found in FDA approved products for the treatment of male sexual enhancement, making this an unapproved drug.
Published: March 23, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Fentanyl 150 mcg/mL Infusion Solution in 250 mL bags, Rx only, Family Pharmacy of Statesville, Inc.

by Family Pharmacy of Statesville

Reason: Lack of Assurance of Sterility
Published: March 23, 2022
Distribution: NC only

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FDA Recall Terminated Historical recordClass II

Methylcobalamin 1 mg/mL Injectable in 1 mL syringes, Rx only, Family Pharmacy of Statesville, Inc.

by Family Pharmacy of Statesville

Reason: Lack of Assurance of Sterility
Published: March 23, 2022
Distribution: NC only

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FDA Recall Terminated Historical recordClass II

Lorazepam 1 mg/mL Infusion Solution in 250 mL bags, Rx only, Family Pharmacy of Statesville, Inc.

by Family Pharmacy of Statesville

Reason: Lack of Assurance of Sterility
Published: March 23, 2022
Distribution: NC only

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FDA Recall Terminated Historical recordClass II

Ketamine 50 mg Infusion (LV 1) Solution in 250 mL bags, Rx only, Family Pharmacy of Statesville, Inc.

by Family Pharmacy of Statesville

Reason: Lack of Assurance of Sterility
Published: March 23, 2022
Distribution: NC only

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FDA Recall Terminated Historical recordClass II

Morphine Sulfate 6 mg/mL Infusion in 250 mL bag, Rx only, Family Pharmacy of Statesville, Inc.

by Family Pharmacy of Statesville

Reason: Lack of Assurance of Sterility
Published: March 23, 2022
Distribution: NC only

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FDA Recall Terminated Historical recordClass II

Vancomycin14 mg/mL Fortified Ophthalmic Solution in 5 mL bottles, Rx only, Family Pharmacy of Statesville, Inc.

by Family Pharmacy of Statesville

Reason: Lack of Assurance of Sterility
Published: March 23, 2022
Distribution: NC only

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FDA Recall Terminated Historical recordClass II

Trimix (Alprostadil/Papaverine/Phentolamine) 10 mcg/20 mg/1 mg Injectable 5 mL vials, Rx only, Family Pharmacy of Statesville, Inc.

by Family Pharmacy of Statesville

Reason: Lack of Assurance of Sterility
Published: March 23, 2022
Distribution: NC only

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FDA Recall Terminated Historical recordClass II

Trimix (Alprostadil/Papaverine/Phentolamine) 20 mcg/30 mg/0.5 mg Injectable 5 mL vials, Rx only, Family Pharmacy of Statesville, Inc.

by Family Pharmacy of Statesville

Reason: Lack of Assurance of Sterility
Published: March 23, 2022
Distribution: NC only

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FDA Recall Terminated Historical recordClass II

Hydromorphone HCl 0.1 mg/mL Infusion in 1000 mL bags, Rx only, Family Pharmacy of Statesville, Inc.

by Family Pharmacy of Statesville

Reason: Lack of Assurance of Sterility
Published: March 23, 2022
Distribution: NC only

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FDA Recall Terminated Historical recordClass II

Hydromorphone HCl 5 mg/mL Infusion in 250 mL bags, Rx only, Family Pharmacy of Statesville, Inc.

by Family Pharmacy of Statesville

Reason: Lack of Assurance of Sterility
Published: March 23, 2022
Distribution: NC only

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FDA Recall Terminated Historical recordClass II

Hydromorphone HCl 1 mg/mL 250 mL bags, Rx only, Family Pharmacy of Statesville, Inc.

by Family Pharmacy of Statesville

Reason: Lack of Assurance of Sterility
Published: March 23, 2022
Distribution: NC only

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FDA Recall Terminated Historical recordClass II

Hydromorphone HCl 2 mg/mL Infusion 250 mL bags, Rx only, Family Pharmacy of Statesville, Inc.

by Family Pharmacy of Statesville

Reason: Lack of Assurance of Sterility
Published: March 23, 2022
Distribution: NC only

View recall →

Data last updated: September 17, 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.