FDA Recall United States Terminated Historical recordClass II
High Liner Foods Inc.
- Product
- Safeway 12/12oz Precooked Sweet Potato Cod Portion 6oz., Ite…
- Reason
- Product may contain undeclared milk.
- Published
- August 23, 2017
- Distribution
- Nationwide
Data Explorer
Research historical outbreak investigations and the full recall archive, with charts, trends, and advanced filters. Looking for what's happening right now instead? See current Health Alerts.
Recall totals
All FDA and USDA recalls in Public Health Trace, June 2012 to September 2026.
37,118
Total recall recordsAll FDA and USDA recalls in Public Health Trace9,793
Class I recallsReasonable probability of serious health consequences24,343
Class II recallsTemporary or medically reversible health consequences2,887
Class III recallsNot likely to cause adverse health consequencesQuick 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/gf-blends-recalls-truly-aip-all-purpose-flour-and-bread-mix-and-eat-gangster-flat-bread-pizza-mixPublished September 18, 2026
Download matching recalls as CSV
CSV exports include up to 5,000 matching rows (applying your current filters), not the full dataset if it's larger.
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A chart of recalls grouped by month.
Download CSVSummary (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
A bar chart of the total number of recalls in this dataset by recall class.
| Class | Recalls |
|---|---|
| Class II | 24,343 |
| Class I | 9,793 |
| Class III | 2,887 |
| Not Yet Classified | 1 |
| Class | Recalls |
|---|---|
| Class II | 24,343 |
| Class I | 9,793 |
| Class III | 2,887 |
| Not Yet Classified | 1 |
FDA Recall United States Terminated Historical recordClass II
High Liner Foods Inc.
- Product
- Trader Joe's 24/16oz Reduced Fat Precooked Crunchy Breaded M…
- Reason
- Product may contain undeclared milk.
- Published
- August 23, 2017
- Distribution
- Nationwide
FDA Recall United States Terminated Historical recordClass II
High Liner Foods Inc.
- Product
- HLSC 12/10oz Coconut Crusted Tilapia, Item Number: 1089431
- Reason
- Product may contain undeclared milk.
- Published
- August 23, 2017
- Distribution
- Nationwide
FDA Recall United States Terminated Historical recordClass II
High Liner Foods Inc.
- Product
- HLSC 12/10oz Summer Herb Crusted Cod Item Number: 1029449
- Reason
- Product may contain undeclared milk.
- Published
- August 23, 2017
- Distribution
- Nationwide
FDA Recall United States Terminated Historical recordClass II
High Liner Foods Inc.
- Product
- HFS 10/6lb Breaded Crispy Style Cod Fish Portions 4 oz., Ite…
- Reason
- Product may contain undeclared milk.
- Published
- August 23, 2017
- Distribution
- Nationwide
FDA Recall United States Terminated Historical recordClass II
High Liner Foods Inc.
- Product
- Viking 12/1lb Precooked Breaded Haddock Fillets 4 oz, Item N…
- Reason
- Product may contain undeclared milk.
- Published
- August 23, 2017
- Distribution
- Nationwide
FDA Recall United States Terminated Historical recordClass II
High Liner Foods Inc.
- Product
- Big Y 12/25oz Breaded Minced Fish Sticks; Item Number: B1202…
- Reason
- Product may contain undeclared milk.
- Published
- August 23, 2017
- Distribution
- Nationwide
FDA Recall United States Terminated Historical recordClass II
High Liner Foods Inc.
- Product
- Best Choice 12/12oz Breaded Minced Fish Sticks; Item Number:…
- Reason
- Product may contain undeclared milk.
- Published
- August 23, 2017
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Hydromorphone Hydrochloride Injection, USP, 50 mg/5 mL (10 mg/mL), 5 mL Single Dose Vial.(10 vials per carton NDC 0703-0113-01) and 180 vials per case (NDC 0703-0113-03) Mfd By: Hospira, Inc., Lake Forest, IL 60045 USA, Mfd For: Teva Parenteral Medicines, Inc., Irvine, CA 92618 USA.
- Reason
- Presence of Particulate Matter: Silicone oil
- Published
- August 16, 2017
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Hydromorphone Hydrochloride Injection, USP, 500 mg/50 mL (10 mg/mL), 50 mL Single Dose Vial per Carton, 100 vials per case. Hospira, Inc., Lake Forest, IL 60045 USA, NDC: 0409-2634-50
- Reason
- Presence of Particulate Matter: Silicone oil
- Published
- August 16, 2017
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Hydromorphone Hydrochloride Injection, USP, 500 mg/50 mL (10 mg/mL), 50 mL Single Dose Vial. Mfd For: Teva Parenteral Medicines, Inc., Irvine, CA 92618 USA. NDC: 0703-0018-01
- Reason
- Presence of Particulate Matter: Silicone oil
- Published
- August 16, 2017
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Rocuronium Bromide Injection Solution 5 mL, 50 mg/5 mL (10 mg/mL) Single-Dose Syringe, Rx Only, Cantrell Drug Company 7321 Cantrell Rd. Little Rock, AR 72207 877-666-5222, NDC 52533-064-15
- Reason
- Lack of Sterility Assurance.
- Published
- August 16, 2017
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Neostigmine Methylsulfate Injection Solution 5 mL, 5 mg/5 mL (1 mg/mL) Single-Dose Syringe, Rx Only, Cantrell Drug Company 7321 Cantrell Rd. Little Rock, AR 72207 877-666-5222, NDC 52533-046-15
- Reason
- Lack of Sterility Assurance.
- Published
- August 16, 2017
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Adenosine in 0.9% Sodium Chloride 30mL, 90 mg/30 mL (3 mg/mL) Single-Dose Syringe, Rx Only, Cantrell Drug Company 7321 Cantrell Rd. Little Rock, AR 72207 877-666-5222; NDC 52533-236-03
- Reason
- Lack of Sterility Assurance.
- Published
- August 16, 2017
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Sodium Bicarbonate 8.4% Injection Solution 50 mL, 50 mEq (1mEq/mL) Single-Dose Syringe, Rx Only, Cantrell Drug Company 7321 Cantrell Rd. Little Rock, AR 72207 877-666-5222
- Reason
- Lack of Sterility Assurance.
- Published
- August 16, 2017
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Phenylephrine HCL in 0.9% Sodium Chloride 10 mL, 1 mg/10 mL (100 mcg/mL) Single-Dose Syringe, Rx Only, Cantrell Drug Company 7321 Cantrell Rd. Little Rock, AR 72207 877-666-5222, NDC 52533-171-12
- Reason
- Lack of Sterility Assurance.
- Published
- August 16, 2017
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Diltiazem HCl 125 mg in 5% Dextrose 125 mL Single-Dose- Bag, Rx Only, Cantrell Drug Company 7321 Cantrell Rd. Little Rock, AR 72207 877-666-5222; NDC 52533-103-13
- Reason
- Lack of Sterility Assurance.
- Published
- August 16, 2017
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Norepinephrine Bitartrate 4 mg Added to 0.9% Sodium Chloride 250 mL (16 mcg per mL) Single-Dose Bag, Rx Only, Cantrell Drug Company 7321 Cantrell Rd. Little Rock, AR 72207 877-666-5222, NDC 52533-134-18
- Reason
- Lack of Sterility Assurance.
- Published
- August 16, 2017
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Norepinephrine Bitartrate 16 mg Added to 0.9% Sodium Chloride 250 mL (64 mcg per mL) Single-Dose Bag, Rx Only, Cantrell Drug Company 7321 Cantrell Rd. Little Rock, AR 72207 877-666-5222, NDC 52533-288-18
- Reason
- Lack of Sterility Assurance.
- Published
- August 16, 2017
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Norepinephrine Bitartrate 8 mg Added to 0.9% Sodium Chloride 250 mL (32 mcg per mL) Single-Dose Bag, Rx Only, Cantrell Drug Company 7321 Cantrell Rd. Little Rock, AR 72207 877-666-5222, NDC 52533-217-18
- Reason
- Lack of Sterility Assurance.
- Published
- August 16, 2017
- Distribution
- Nationwide
Data last updated:
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.
