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Recall totals

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

37,211

Total recall recordsAll FDA and USDA recalls in Public Health Trace

9,841

Class I recallsReasonable probability of serious health consequences

24,366

Class II recallsTemporary or medically reversible health consequences

2,892

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 2,073 recalls

Newest recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/frutas-y-hortalizas-del-sur-sa-expands-recalls-include-additional-lots-great-value-frozen-organicPublished October 2, 2026

Most affected stateHawaii 200 recalls mention this state

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

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Source: FDA and USDA public dataLast updated October 3, 2026 ET

Summary (Year to date)

1,714 recalls have been announced year to date.
Sep 2026 was 3% higher than the previous complete period (Aug 2026: 182).
The highest complete period was Jun 2026 (297).
Oct 2026 is incomplete and not included in the figures above.

Complete data
Incomplete

Recalls by class

Recalls by class
Class	Recalls
Class II	24,366
Class I	9,841
Class III	2,892
Not Yet Classified	2

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Recalls by class
Class	Recalls
Class II	24,366
Class I	9,841
Class III	2,892
Not Yet Classified	2

FDA Recall Terminated Historical recordClass II

PGE-1 Inj 20mcg/ml MDV: 5ml, 7ml, 10ml, 20ml Penile Injection, 90 day expiration,

by Nora Apothecary and Alternative Therapies, Inc.

Reason: Lack of Assurance of Sterility: FDA inspection findings resulted in concerns regarding quality control processes.
Published: June 5, 2013
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

PGE-1 Inj 10mcg/ml MDV, 5ml Penile Injection, 90 day expiration,

by Nora Apothecary and Alternative Therapies, Inc.

Reason: Lack of Assurance of Sterility: FDA inspection findings resulted in concerns regarding quality control processes.
Published: June 5, 2013
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Papaverine Inj 30mg/ml Syr, 5mlsyr, 10mlsyr,10x0.95mlsyr Penile Injection, 90 day expiration,

by Nora Apothecary and Alternative Therapies, Inc.

Reason: Lack of Assurance of Sterility: FDA inspection findings resulted in concerns regarding quality control processes.
Published: June 5, 2013
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Bimix Inj 30:1 MDV: 5ml, 10 ml, 3x10ml, 2x10ml Penile Injection, 30 and 90 day expiration,

by Nora Apothecary and Alternative Therapies, Inc.

Reason: Lack of Assurance of Sterility: FDA inspection findings resulted in concerns regarding quality control processes.
Published: June 5, 2013
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Bimix Inj 30:0.5 MDV, 5 ml syr Penile Injection, 90 day expiration,

by Nora Apothecary and Alternative Therapies, Inc.

Reason: Lack of Assurance of Sterility: FDA inspection findings resulted in concerns regarding quality control processes.
Published: June 5, 2013
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Bimix Inj 30 :1 Syr, 12x1.5 ml syr, 10x1.2 ml syr, 2x2 ml syr, 2x1 ml syr, 12x.05 ml syr Penile Injection,30 and 90 day expiration,

by Nora Apothecary and Alternative Therapies, Inc.

Reason: Lack of Assurance of Sterility: FDA inspection findings resulted in concerns regarding quality control processes.
Published: June 5, 2013
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Renacidin Irrigation: 1000 ml,1120ml Bladder Irrigation, 30 day expiration,

by Nora Apothecary and Alternative Therapies, Inc.

Reason: Lack of Assurance of Sterility: FDA inspection findings resulted in concerns regarding quality control processes.
Published: June 5, 2013
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Budesonide Capsules, 3 mg, Enteric Coated, packaged in 30-count capsules unit dose (3 x 10 capsules blister packaged) per box, Rx only, Manufactured by: Mylan Pharmaceuticals Inc., Morgantown, WV 26505; Packaged and Distributed by: UDL Laboratories, Inc., Rockford, IL 61103, NDC 51079-020-03.

by Mylan Institutional, Inc. (d.b.a. UDL Laboratories)

Reason: Failed Dissolution Specifications: Routine stability testing at the 12-month interval yielded an out-of-specification (OOS) result for dissolution testing.
Published: May 29, 2013
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Levothroid (levothyroxine sodium tablets, USP), 200 mcg, RX only, 100 tablets per bottle. Manufactured for Forest Pharmaceuticals, Inc, St. Louis, MO by Lloyd Pharmaceutical, Shenandoah, IA, NDC 0456-1327-01

by Lloyd Inc. of Iowa

Reason: cGMP deviations; After quality review of stability failures in previous lots, there is insufficient data to determine that other lots are not affected.
Published: May 29, 2013
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Levothroid (levothyroxine sodium tablets, USP), 175 mcg, RX only, 100 tablets per bottle, Manufactured for Forest Pharmaceuticals, Inc, St. Louis, MO by Lloyd Pharmaceutical, Shenandoah, IA, NDC 0456-1326-01

by Lloyd Inc. of Iowa

Reason: cGMP deviations; After quality review of stability failures in previous lots, there is insufficient data to determine that other lots are not affected.
Published: May 29, 2013
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Levothroid (levothyroxine sodium tablets, USP), 150 mcg, RX only, 100 tablets per bottle, Manufactured for Forest Pharmaceuticals, Inc, St. Louis, MO by Lloyd Pharmaceutical, Shenandoah, IA, NDC 0456-1325-01.

by Lloyd Inc. of Iowa

Reason: cGMP deviations; After quality review of stability failures in previous lots, there is insufficient data to determine that other lots are not affected.
Published: May 29, 2013
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Levothroid (levothyroxine sodium tablets, USP), 137 mcg, RX only, 100 tablets per bottle, Manufactured for Forest Pharmaceuticals, Inc, St. Louis, MO by Lloyd Pharmaceutical, Shenandoah, IA, NDC 0456-1331-01.

by Lloyd Inc. of Iowa

Reason: cGMP deviations; After quality review of stability failures in previous lots, there is insufficient data to determine that other lots are not affected.
Published: May 29, 2013
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Levothroid (levothyroxine sodium tablets, USP) , 125 mcg, RX only, 100 tablets per bottle, Manufactured for Forest Pharmaceuticals, Inc, St. Louis, MO by Lloyd Pharmaceutical, Shenandoah, IA, NDC 0456-1324-01

by Lloyd Inc. of Iowa

Reason: cGMP deviations; After quality review of stability failures in previous lots, there is insufficient data to determine that other lots are not affected.
Published: May 29, 2013
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Levothroid (levothyroxine sodium tablets, USP), 112 mcg, RX only, 100 tablets per bottle, Manufactured for Forest Pharmaceuticals, Inc, St. Louis, MO by Lloyd Pharmaceutical, Shenandoah, IA, NDC 0456-1330-01

by Lloyd Inc. of Iowa

Reason: cGMP deviations; After quality review of stability failures in previous lots, there is insufficient data to determine that other lots are not affected.
Published: May 29, 2013
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Levothroid (levothyroxine sodium tablets, USP), 100 mcg, RX only, 100 tablets per bottle, Manufactured for Forest Pharmaceuticals, Inc, St. Louis, MO by Lloyd Pharmaceutical, Shenandoah, IA, NDC 0456-1323-01

by Lloyd Inc. of Iowa

Reason: cGMP deviations; After quality review of stability failures in previous lots, there is insufficient data to determine that other lots are not affected.
Published: May 29, 2013
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Lloyd Thyro-Tab 0.200 mg., packaged in 150,000-tablet bulk drums (2/75,000-tablet bags/drum) for repackaging, RX. The firm name on the label is Lloyd Pharmaceutical, Shenandoah, IA.

by Lloyd Inc. of Iowa

Reason: cGMP deviations; After quality review of stability failures in previous lots, there is insufficient data to determine that other lots are not affected.
Published: May 29, 2013
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Lloyd Thyro-Tab 0.175 mg., packaged in 150,000-tablet bulk drums (2/75,000-tablet bags/drum) for repackaging, RX. The firm name on the label is Lloyd Pharmaceutical, Shenandoah, IA.

by Lloyd Inc. of Iowa

Reason: cGMP deviations; After quality review of stability failures in previous lots, there is insufficient data to determine that other lots are not affected.
Published: May 29, 2013
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Lloyd Thyro-Tab 0.150 mg., packaged in 150,000-tablet bulk drums (2/75,000-tablet bags/drum) for repackaging, RX. The firm name on the label is Lloyd Pharmaceutical, Shenandoah, IA.

by Lloyd Inc. of Iowa

Reason: cGMP deviations; After quality review of stability failures in previous lots, there is insufficient data to determine that other lots are not affected.
Published: May 29, 2013
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Lloyd Thyro-Tab 0.137 mg., packaged in 150,000-tablet bulk drums (2/75,000-tablet bags/drum) for repackaging, RX. The firm name on the label is Lloyd Pharmaceutical, Shenandoah, IA.

by Lloyd Inc. of Iowa

Reason: cGMP deviations; After quality review of stability failures in previous lots, there is insufficient data to determine that other lots are not affected.
Published: May 29, 2013
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Lloyd Thyro-Tab 0.125 mg., packaged in 150,000-tablet bulk drums (2/75,000-tablet bags/drum) for repackaging, RX. The firm name on the label is Lloyd Pharmaceutical, Shenandoah, IA.

by Lloyd Inc. of Iowa

Reason: cGMP deviations; After quality review of stability failures in previous lots, there is insufficient data to determine that other lots are not affected.
Published: May 29, 2013
Distribution: Nationwide

View recall →

Data last updated: October 3, 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.