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Recall totals

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

37,142

Total recall recordsAll FDA and USDA recalls in Public Health Trace

9,799

Class I recallsReasonable probability of serious health consequences

24,349

Class II recallsTemporary or medically reversible health consequences

2,891

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 recallhttps://www.fsis.usda.gov/recalls-alerts/fontanini-foods-llc-recalls-raw-frozen-pork-sausage-products-due-possible-foreignPublished September 25, 2026

Most affected stateHawaii 200 recalls mention this state

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

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Source: FDA and USDA public dataLast updated September 26, 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	24,349
Class I	9,799
Class III	2,891
Not Yet Classified	1

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Recalls by class
Class	Recalls
Class II	24,349
Class I	9,799
Class III	2,891
Not Yet Classified	1

FDA Recall Terminated Historical recordClass II

oxyTOCIN 30 units added to Lactated Ringers 500 mL Bag, Rx Only, SCA Pharmaceuticals 8821 Knoedl Ct Little Rock, AR 72205, NDC 70004-0086-44

by SCA Pharmaceuticals, LLC

Reason: Lack Of Assurance Of Sterility.
Published: November 8, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

morphine sulfate 1 mg per mL in 0.9% Sodium Chloride a) Total Volume 100 mL in Single Dose CADD Cassette (Total morphine Dose 100 mg per 100 mL) (NDC 70004-0100-63) b) Total Volume 50 mL in Single Dose Syringe (Total morphine Dose 50 mg / 50 mL) (NDC 70004-0100-22) Rx Only, SCA Pharmaceuticals 8821 Knoedl Ct Little Rock, AR 72205

by SCA Pharmaceuticals, LLC

Reason: Lack Of Assurance Of Sterility.
Published: November 8, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

fentaNYL as citrate 2 mcg / mL, ROPIVacaine HCl 0.1%, Total Fentanyl Dose (200 mcg per 100 mL) in 0.9% Sodium Chloride single dose CADD Cassette Rx Only, SCA Pharmaceuticals 8821 Knoedl Ct Little Rock, AR 72205, NDC 70004-0264-64

by SCA Pharmaceuticals, LLC

Reason: Lack Of Assurance Of Sterility.
Published: November 8, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

fentanyl as citrate 2 mcg per mL BUPIvacaine HCl 0.125% (Total FentaNYL Dose 500 mcg/250 mL) in 0.9% Sodium Chloride 250 mL Bag, Rx Only, SCA Pharmaceuticals, 8821 Knoedl Ct, Little Rock, AR 72205. NDC 70004-0231-40

by SCA Pharmaceuticals, LLC

Reason: Lack Of Assurance Of Sterility.
Published: November 8, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

HYDROmorphone HCl 20 mcg / mL BUPIvacaine HCl 0.075% in 0.9% Sodium Chloride 50 mL (HYDROmorphone Total Dose 1000 mcg) Rx Only, SCA Pharmaceuticals 8821 Knoedl Ct Little Rock, AR 72205, NDC 70004-0331-22

by SCA Pharmaceuticals, LLC

Reason: Lack Of Assurance Of Sterility.
Published: November 8, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

HYDROmorphone HCL 1 mg per mL in 0.9% Sodium Chloride 25 mL Fill in 30 mL single-dose syringe (Total Dose Hydromorphone 25 mg/25 mL) Rx Only SCA Pharmaceuticals 8821 Knoedl Ct Little Rock, AR NDC 70004-0303-17

by SCA Pharmaceuticals, LLC

Reason: Lack Of Assurance Of Sterility.
Published: November 8, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

SUCcinylcholine 20 mg per mL, Total Volume 10 mL in single-dose syringe, (SUCcinylcholine 200 mg / 10 ml) Rx Only, SCA Pharmaceuticals 8821 Knoedl Ct Little Rock, AR NDC 70004-0910-29

by SCA Pharmaceuticals, LLC

Reason: Lack Of Assurance Of Sterility.
Published: November 8, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

A1 Slim, Dietary Supplement Beautifully Slim, capsule, 350 mg, 30-count bottle, A1 Slim LLC Pearland TX 77584, www.A1SLIM.COM, info@a1slim.com Bar-Code A105212014

by Kiriko, LLC.

Reason: Marketed Without An Approved NDA/ANDA: FDA analysis found this product to contain undeclared sibutramine, phenolphthalein, and n-desmethyl sibutramine, making this an unapproved drug for which safety and efficacy have not been established and therefore, subject to recall.
Published: November 8, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Carbamazepine Oral Suspension USP, 100 mg/5 mL, 5 mL Unit Dose Cups (NDC 68094-301-59), packaged in 10-count cups per tray, 3 trays per case containing a total of 5 mL x 30 Unit Dose Cups per case (NDC 68094-301-62), Rx only, Pkg: Precision Dose, Inc., S. Beloit, IL 61080.

by Precision Dose Inc.

Reason: Subpotent Drug: low out of specification results.
Published: November 8, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Clofarabine injection, 20 mg/20 mL, 20 mL Single-Use Vial, Rx only, Mfd by: Teva Pharmachemle, Swensweg 5, Haarlem, The Netherlands; Mfd for: Winthrop U.S., a business of sanofi-aventis U.S. LLC, Bridgewater, NJ 08807; NDC 0955-1746-01.

by Sanofi-Aventis U.S. LLC

Reason: Labeling: Incorrect or Missing Package Insert: authorized generic product was packaged with the incorrect insert for the brand name product Clolar (clofarabine) injection.
Published: November 8, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Duloxetine Delayed-release Capsules USP, 20 mg, 50 Capsules (5 x 10) Unit Dose per carton, unit dose blister UPC 5026828311), Rx only, Manufactured for: AvKARE, Inc., Pulaski, TN 38478, NDC 50268-283-15.

by AVKARE Inc.

Reason: Failed Impurities/Degradation Specifications: slightly elevated levels of phthalic acid.
Published: November 8, 2017
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Triple B Corporation

Product: Veggie Tray w/Dip (12"), Alaska Carrot brand, 2 x 32 oz. pe…
Reason: Veggie Tray w/Dip product is recalled due to possible contamination with Listeria monocytogenes. The broccoli used in processing this item has been recalled by vendor Mann Packing of Salinas, California.
Published: November 8, 2017
Distribution: distributed in Alaska, Idaho, Montana, O…

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FDA Recall United States Terminated Historical recordClass I

Triple B Corporation

Product: Veggie Medley, Alaska Carrot, 12 x 16 oz. per case, UPC 45…
Reason: Veggie Medley product is recalled due to possible contamination with Listeria monocytogenes. The broccoli used in processing this item has been recalled by vendor Mann Packing of Salinas, California.
Published: November 8, 2017
Distribution: distributed in Alaska, Idaho, Montana, O…

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FDA Recall United States Terminated Historical recordClass I

Triple B Corporation

Product: Broccoli Florette, Alaska Carrot brand, 1 x 3 lb. per case,…
Reason: Broccoli Florette product is recalled due to possible contamination with Listeria monocytogenes. The broccoli used in processing this item has been recalled by vendor Mann Packing of Salinas, California.
Published: November 8, 2017
Distribution: distributed in Alaska, Idaho, Montana, O…

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FDA Recall United States Terminated Historical recordClass I

Triple B Corporation

Product: Stir Fry (GL) 4 x 10 oz. per case, UPC 45009 85367 7. Stir…
Reason: Stir Fry product is recalled due to possible contamination with Listeria monocytogenes. The broccoli used in processing this item has been recalled by vendor Mann Packing of Salinas, California.
Published: November 8, 2017
Distribution: distributed in Alaska, Idaho, Montana, O…

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FDA Recall United States Terminated Historical recordClass I

Triple B Corporation

Product: Kit, Thai Veggie, Produced by CP Fresh of Seattle, WA, 1 x 5…
Reason: Kit, Thai Veggie is recalled due to possible contamination with Listeria monocytogenes. The broccoli used in processing this item has been recalled by vendor Mann Packing of Salinas, California.
Published: November 8, 2017
Distribution: distributed in Alaska, Idaho, Montana, O…

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FDA Recall United States Terminated Historical recordClass I

Triple B Corporation

Product: Broccoli Salad Kit, Produced by CP Fresh of Seattle, WA, 1 x…
Reason: Down-stream from Mann Packing recall #78326. Broccoli Salad Kit is recalled due to possible contamination with Listeria monocytogenes. The broccoli used in processing this item has been recalled by vendor Mann Packing of Salinas, California.
Published: November 8, 2017
Distribution: distributed in Alaska, Idaho, Montana, O…

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FDA Recall United States Terminated Historical recordClass I

Triple B Corporation

Product: Asparagus Salad Kit, Produced by CP Fresh of Seattle, WA, 1…
Reason: Asparagus Salad Kit is recalled due to possible contamination with Listeria monocytogenes. The broccoli used in processing this item has been recalled by vendor Mann Packing of Salinas, California.
Published: November 8, 2017
Distribution: distributed in Alaska, Idaho, Montana, O…

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FDA Recall United States Terminated Historical recordClass I

Earthbound Farm, LLC

Product: Earthbound Farm¿ Organic Chopped Asian Style Salad Kit; 11 o…
Reason: Recall of Asian Style Chopped Salad Kit because in some instances the dressing and toppings packets inside the bag are not those foe the salad. Some of the Asian Style Salad Kits could have the dressing packet for the Southwest Chopped Salad Kit which contains egg and milk that are not declared as ingredients on the bag of the Asian Style Salad Kit.
Published: November 8, 2017
Distribution: Alaska, Arizona, California, Colorado, F…

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FDA Recall United States Terminated Historical recordClass I

Organic Spices, Inc

Product: Spicely Organics Organic Tarragon 0.4oz. (11g) UPC codes:…
Reason: Potential Salmonella contamination.
Published: November 8, 2017
Distribution: U.S. distribution to the following: Alas…

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Data last updated: September 26, 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.