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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: VT ×
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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

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

Maximum Strength No Drip Nasal Spray, Oxymetazoline HCl 0.05% Nasal Decongestant, 1 FL Oz (30 mL) per bottle, DISTRIBUTED BY: AMAZON.COM SERVICES LLC, 410 TERRY AVENUE N. SEATTLE, WA 9810. NDC 72288-388-10

by Perrigo Company PLC

Reason: CGMP Deviations: Products were manufactured with contaminated excipient that was recalled from the excipient supplier.
Published: March 2, 2022
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Maximum Strength No Drip Nasal Spray, Oxymetazoline HCl 0.05% Nasal Decongestant, 1 FL Oz (30 mL) per bottle, DISTRIBUTED BY: AMAZON.COM SERVICES LLC, 410 TERRY AVENUE N. SEATTLE, WA 9810. NDC 72288-388-10

by Perrigo Company PLC

Reason: CGMP Deviations: Products were manufactured with contaminated excipient that was recalled from the excipient supplier.
Published: March 2, 2022
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Severe Congestion Nasal Spray, No Drip Plus Menthol, Oxymetazoline HCl 0.05%, 1 FL Oz (30 mL) per bottle, DISTRIBUTED BY TOPCO ASSOCIATES LLC., ELK GROVE VILLAGE, IL 60007. NDC 36800-907-10

by Perrigo Company PLC

Reason: CGMP Deviations: Products were manufactured with contaminated excipient that was recalled from the excipient supplier.
Published: March 2, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Severe Congestion Nasal Spray, No Drip Plus Menthol, Oxymetazoline HCl 0.05%, 1 FL Oz (30 mL) per bottle, Dist. by Target Corp., Mpls., MN 55403. NDC 11673-935-10

by Perrigo Company PLC

Reason: CGMP Deviations: Products were manufactured with contaminated excipient that was recalled from the excipient supplier.
Published: March 2, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Severe Congestion Nasal Spray, No Drip Plus Menthol, Oxymetazoline HCl 0.05%, 1 FL Oz (30 mL) per bottle, Distributed by SUPERVALU INC., Eden Prairie, MN 55344 USA. NDC 41163-343-10

by Perrigo Company PLC

Reason: CGMP Deviations: Products were manufactured with contaminated excipient that was recalled from the excipient supplier.
Published: March 2, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Severe Congestion Nasal Spray, No Drip Plus Menthol, Oxymetazoline HCl 0.05%, 1 FL Oz (30 mL) per bottle, DISTRIBUTED BY: BETTER LIVING BRANDS LLC, P.O. BOX 99, PLEASANTON, CA 94566-0009. NDC 21130-813-10

by Perrigo Company PLC

Reason: CGMP Deviations: Products were manufactured with contaminated excipient that was recalled from the excipient supplier.
Published: March 2, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Severe Congestion Nasal Spray, No Drip Plus Menthol, Oxymetazoline HCl 0.05%, 1 FL Oz (30 mL) per bottle, DISTRIBUTED BY: RITE AID, 30 HUNTER LANE, CAMP HILL, PA 17011. NDC 11822-6378-1

by Perrigo Company PLC

Reason: CGMP Deviations: Products were manufactured with contaminated excipient that was recalled from the excipient supplier.
Published: March 2, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Severe Congestion Nasal Spray, No Drip Plus Menthol, Oxymetazoline HCl 0.05%, 1 FL Oz (30 mL) per bottle, DISTRIBUTED BY FOODHOLD U.S.A., LLC, LANDOVER, MD 20785. NDC 41520-108-10

by Perrigo Company PLC

Reason: CGMP Deviations: Products were manufactured with contaminated excipient that was recalled from the excipient supplier.
Published: March 2, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Severe Congestion No Drip Nasal Spray Plus Menthol, Oxymetazoline HCl 0.05%, 1 FL Oz (30 mL) per bottle, DISTRIBUTED BY DOLGENCORP, LLC, 100 MISSION RIDGE, GOODLETTSVILLE, TN 37072. NDC 55910-511-10

by Perrigo Company PLC

Reason: CGMP Deviations: Products were manufactured with contaminated excipient that was recalled from the excipient supplier.
Published: March 2, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Severe Congestion Nasal Spray, No Drip Plus Menthol, Oxymetazoline HCl 0.05%, 1 FL Oz (30 mL) per bottle, DISTRIBUTED BY FOODHOLD U.S.A., LLC, LANDOVER, MD 20785. NDC 41520-108-10

by Perrigo Company PLC

Reason: CGMP Deviations: Products were manufactured with contaminated excipient that was recalled from the excipient supplier.
Published: March 2, 2022
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Severe Congestion Nasal Spray, No Drip Plus Menthol, Oxymetazoline HCl 0.05% Nasal Decongestant, 1 FL Oz (30 mL) per bottle, Packaged by Perrigo Company for: Big Lots Stores, Inc., P.O. Box 28523, Columbus, OH 43228-0523. NDC: 50594-719-10

by Perrigo Company PLC

Reason: CGMP Deviations: Products were manufactured with contaminated excipient that was recalled from the excipient supplier.
Published: March 2, 2022
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Maximum Strength Plus Menthol No Drip Nasal Spray, Oxymetazoline HCl 0.05% Nasal Decongestant, 1 FL Oz (30 mL) per bottle, DISTRIBUTED BY: AMAZON.COM SERVICES LLC 410 TERRY AVENUE N.SEATTLE, WA 98109. NDC: 72288-703-10

by Perrigo Company PLC

Reason: CGMP Deviations: Products were manufactured with contaminated excipient that was recalled from the excipient supplier.
Published: March 2, 2022
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Acetaminophen Child Bubble Gum Flavored Oral Suspension (160 mg/5 ml), 4 FL OZ (118 mL) per bottle, Distributed by Perrigo, Allegan, MI 49010. NDC: 0113-0020-26

by Perrigo Company PLC

Reason: CGMP Deviations: Products were manufactured with contaminated excipient that was recalled from the excipient supplier.
Published: March 2, 2022
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Acetaminophen Child Bubble Gum Flavored Oral Suspension (160 mg/5 ml), 4 FL OZ (118 mL) per bottle, Distributed by Perrigo, Allegan, MI 49010. NDC: 11673-105-26

by Perrigo Company PLC

Reason: CGMP Deviations: Products were manufactured with contaminated excipient that was recalled from the excipient supplier.
Published: March 2, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Children's Pain & Fever Acetaminophen, 160 mg per 5 mL Oral Suspension combo pack. DS SR APAP 160MG CHLD BBGM/DF CHRY/GRP. UPC: 3 70030 11637 9

by Perrigo Company PLC

Reason: CGMP Deviations: Products were manufactured with contaminated excipient that was recalled from the excipient supplier.
Published: March 2, 2022
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Acetaminophen Child Bubble Gum Flavored Oral Suspension (160 mg/5 ml), two 4 FL OZ (118 mL) bottles per pack, Distributed by Walmart Inc., Bentonville, AR 72716. NDC: 49035-313-26

by Perrigo Company PLC

Reason: CGMP Deviations: Products were manufactured with contaminated excipient that was recalled from the excipient supplier.
Published: March 2, 2022
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Infant's Grape Flavored Acetaminophen Oral Suspension (160mg/5ml), 2 FL OZ (59 mL) per bottle, DISTRIBUTED BY: Wal-Mart Stores, Inc., Bentonville, AR 72716. NDC: 49035-946-16

by Perrigo Company PLC

Reason: CGMP Deviations: Products were manufactured with contaminated excipient that was recalled from the excipient supplier.
Published: March 2, 2022
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Acetaminophen Infant Dye Free Grape Oral Suspension (160mg/5ml), 2 FL OZ (59 mL) per bottle, DISTRIBUTED BY: Wal-Mart Stores, Inc., Bentoneville, AR 72716. NDC: 49035-766-16

by Perrigo Company PLC

Reason: CGMP Deviations: Products were manufactured with contaminated excipient that was recalled from the excipient supplier.
Published: March 2, 2022
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Acetaminophen Infant Dye Free Grape Oral Suspension (160mg/5ml), 2 FL OZ (59 mL) per bottle, DISTRIBUTED BY THE KROGER CO., CINCINNATI, OHIO 45202. NDC: 30142-766-16

by Perrigo Company PLC

Reason: CGMP Deviations: Products were manufactured with contaminated excipient that was recalled from the excipient supplier.
Published: March 2, 2022
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Acetaminophen Infant Dye Free Grape Oral Suspension (160mg/5ml), 2 FL OZ (59 mL) per bottle, DISTRIBUTED BY THE KROGER CO., CINCINNATI, OHIO 45202. NDC: 30142-766-16

by Perrigo Company PLC

Reason: CGMP Deviations: Products were manufactured with contaminated excipient that was recalled from the excipient supplier.
Published: March 2, 2022
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.