Recalls

All US Product Recalls

Searchable archive of product recalls from the FDA, USDA FSIS, CPSC, NHTSA, and EPA — translated into plain English, severity-scored from objective criteria, and always linked back to the original government notice.

How to read this listing

Every recall on this list has been scored 1–5 against an objective rubric from the agency’s own classification, presence of reported injuries or deaths, distribution scope, and hazard type. The colored severity badge on each card is the score — 5 (Critical) means the agency’s own highest classification or reported deaths or serious injuries, 4 (Severe) means significant injury or hospitalization risk, and 3 (High) means a known hazard with no confirmed harm yet. Filter to 3+ (High and above) if you want to skip routine Class-III notices.

The agency chips above control which streams are visible. FDA spans food, drugs, and medical devices. USDA FSIS is meat, poultry, and processed egg products. CPSC is household consumer products. NHTSA is vehicles, tires, and child seats. Nationwide on a card means the recall affects every US state — most do — while a state list means distribution was limited.

Click any recall to see the full summary, affected lot codes and model numbers, the agency’s own classification, and a direct link back to the original government notice for verification.

Agency

All agencies FDA (Food)FDA (Drugs)FDA (Devices)USDA FSIS CPSC NHTSA EPA

6251–6275 of 7452

CriticalFDA (Devices)·Z-2298-2013·2013-10-09
MedStream Refill Kit Recalled for Excessive Drug Flow Rates
Codman & Shurtleff, Inc. is recalling MedStream Refill Kits because they may deliver drug flow rates exceeding programmed levels.
Product
MedStream Refill Kit, U.S (6 units): 91-4288 Product Usage: The Medstream programmable pump is intended for the intrathecal delivery of Baclofen in the US market and for the intrathecal delivery of Morphine or Baclofen in the EMEA market. Refill Kits- are intended for use in…
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-2295-2013·2013-10-09
MedStream Refill Kit Recalled for Excessive Drug Flow Rates
Codman & Shurtleff is recalling MedStream Refill Kits because they may deliver drug flow rates exceeding programmed levels.
Product
MedStream Refill Kit, U.S: 91-4287 Product Usage: The Medstream programmable pump is intended for the intrathecal delivery of Baclofen in the US market and for the intrathecal delivery of Morphine or Baclofen in the EMEA market. Refill Kits- are intended for use in the…
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Food)·F-1910-2013·2013-10-02
Bubbles Baking Blueberry Muffins Recalled for Undeclared Milk and Soy
Bubbles Baking Co. is recalling First Street Blueberry Muffins Loaf because they may contain undeclared milk and soy allergens.
Product
First Street Blueberry Muffins Loaf (S 45383), 16 oz., 12 trays/case, UPC 0 41512 10854 9.
Category
Food
Distribution
1 state
CriticalFDA (Food)·F-1902-2013·2013-09-25
JTM Provisions Recalls Bean and Cheese Burrito Filling for Undeclared Eggs
JTM Provisions Co Inc is recalling 10 lb bags of Bean & Cheese Burrito Filling because the product contains undeclared eggs.
Product
Bean & Cheese Burrito Filling, 10 lb bags Labeled in part "13210 B 1 77220 13:38 KEEP FROZEN BEAN & CHEESE BURRITO FILLING***INGREDIENTS: COOKED PINTO BEANS, WATER, CHEDDAR CHEESE***SOYBEAN OIL***STARCH-MODIFIED, ONIONS, CHEESE SAUCE BASE***CONTAINS LESS THAN 2% OF CHILI PEPPER…
Category
Food
Distribution
1 state
CriticalFDA (Devices)·Z-2126-2013·2013-09-18
Siemens Microscan Plus Negative Breakpoint Combo 4 Recalled for Misreads
Siemens Healthcare Diagnostics is recalling Microscan plus Negative Breakpoint Combo 4 panels due to confirmed false susceptible and intermediate misreads for specific antibiotics.
Product
Microscan plus Negative Breakpoint Combo 4 Sold outside of US only. Product Usage: MicroScan¿ Synergies plus¿ Panels & MicroScan¿ Rapids plus (Negative) - For use in determining quantitative and/or qualitative antimicrobial agent susceptibility and/or identification…
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-2125-2013·2013-09-18
Siemens Microscan plus Negative Urine Combo 4 Recalled for Misreads
Siemens Healthcare Diagnostics is recalling Microscan plus Negative Urine Combo 4 panels due to confirmed false susceptible and intermediate misreads for specific antibiotics.
Product
Microscan plus Negative Urine Combo 4 Sold outside of US only. Product Usage: MicroScan¿ Synergies plus¿ Panels & MicroScan¿ Rapids plus (Negative) - For use in determining quantitative and/or qualitative antimicrobial agent susceptibility and/or identification for…
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-2123-2013·2013-09-18
Siemens Microscan Synergies Plus Negative Urine Combo 5 Recall
Siemens is recalling Microscan Synergies Plus Negative Urine Combo 5 panels due to confirmed false susceptibility results for imipenem and meropenum.
Product
Microscan Synergies Plus Negative Urine Combo 5 Product Usage: MicroScan¿ Synergies plus¿ Panels & MicroScan¿ Rapids plus (Negative) - For use in determining quantitative and/or qualitative antimicrobial agent susceptibility and/or identification for gram-negative…
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-2124-2013·2013-09-18
Siemens Microscan Plus Negative Combo 3 Recalled for Misreads
Siemens Healthcare Diagnostics is recalling Microscan plus Negative Combo 3 panels due to confirmed false susceptible and intermediate misreads for imipenem and meropenum.
Product
Microscan plus Negative Combo 3 Sold outside of US only. Product Usage: MicroScan¿ Synergies plus¿ Panels & MicroScan¿ Rapids plus (Negative) - For use in determining quantitative and/or qualitative antimicrobial agent susceptibility and/or identification for…
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-929-2013·2013-09-11
FDA Recalls SexVoltz Herbal Supplement Containing Unapproved Tadalafil
Beamonstar Products is recalling SexVoltz All Natural Herbal Supplement because it contains tadalafil, an unapproved drug ingredient.
Product
SexVoltz All Natural Herbal Supplement, packaged in 1 & 2 capsule blister packs and 4, 10 and 12 capsule bottles, Manufactured For: BeaMonstar Products, Queen Creek, AZ
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Food)·F-1865-2013·2013-09-11
Zip International Recalls Baltic Sprats in Spicy Brine Due to Listeria Risk
Zip International Group LLC is recalling Baltic Sprats in Spicy Brine because the product may be contaminated with Listeria monocytogenes.
Product
Baltic Sprats in Spicy Brine Net Wt. 15.8 oz. Prod. of Latvia Distributed by Zip International Group LLC 160 Raritan Center Parkway Unit #6 Edison NJ 08837 T 732-225-3600 UPC 4750217602547
Category
Food
Distribution
1 state
CriticalFDA (Drugs)·D-930-2013·2013-09-11
Velextra Herbal Supplement Recalled for Containing Unapproved Tadalafil
Beamonstar Products is recalling Velextra All-Natural Herbal Supplement because it contains tadalafil, an unapproved drug ingredient.
Product
Velextra All-Natural Herbal Supplement, packaged in 1 & 2 capsule blister packs and 4, 10 & 12 capsule bottles, Manufactured For: BeaMonstar Products Queen Creek, AZ
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Food)·F-1866-2013·2013-09-11
Kroger Cookie Dough Recalled for Undeclared Peanut Allergen
Conagra is recalling Kroger Break 'N Bake Chocolate Chip Cookie Dough because peanut butter was present but not listed on the label.
Product
Kroger Break 'N Bake Chocolate Chip Cookie Dough, refrigerated dough, packaged in 16.0 oz. plastic package.
Category
Food
Distribution
26 states
CriticalFDA (Food)·F-1854-2013·2013-09-04
Heeren Brothers Recalls Athena Cantaloupes Due to Listeria Contamination
Heeren Brothers Produce is recalling Athena cantaloupes sold in Michigan after FDA testing found Listeria monocytogenes contamination.
Product
Cardboard BIN LABEL: 03808 LOT #: 09000101, MELON CANTALOUPE..., 80-90 CT , 07/22/13 cantaloupes themselves are not labeled.
Category
Food
Distribution
1 state
CriticalFDA (Drugs)·D-922-2013·2013-09-04
Hospira Recalls 0.9% Sodium Chloride Injection Due to Particulate Matter
Hospira is recalling 264,432 bags of 0.9% Sodium Chloride Injection because the product may contain fibrous material.
Product
0.9% Sodium Chloride Injection, USP, 100 mL flexible container, Rx only, Hospira, Inc. Lake Forest, IL 60045 --- NDC 0409-7984-23
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-919-2013·2013-09-04
Rugby Enteric Coated Aspirin 81 mg Recalled for Labeling Error
Advance Pharmaceutical Inc. is recalling 16,440 bottles of Enteric Coated Aspirin 81 mg due to a label mix-up where one bottle contained Acetaminophen 500 mg.
Product
ENTERIC COATED ASPIRIN (NSAID), 81 mg, 120-count tablets per bottle, distributed by: Rugby Laboratories, Inc., Duluth, Georgia 30097, NDC 0536-3086-41, UPC 3 0536-3086-41 9.
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Food)·F-1852-2013·2013-09-04
Buurma Farms Cilantro Recalled Due to Listeria monocytogenes Contamination
Buurma Farms is recalling fresh cilantro after a customer reported a positive Listeria monocytogenes test result from the Michigan Department of Agriculture.
Product
Buurma Farms Cilantro, fresh, 4 oz bunch, #4889 UPC 0 33383 80104 9
Category
Food
Distribution
4 states
CriticalFDA (Drugs)·D-921-2013·2013-09-04
Bethel 30 capsules recalled for undeclared active ingredients
Bethel Nutritional Consulting, Inc. is recalling Bethel 30 capsules because FDA analysis found undeclared sibutramine and phenolphthalein, making the product an unapproved new drug.
Product
Bethel 30 capsules, packaged in 30 count bottles, Distributed by BETHEL INC. New York, New York
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-920-2013·2013-09-04
Fresenius Kabi Recalls Magnesium Sulfate Injection Due to Glass Particulates
Fresenius Kabi is recalling 15,625 vials of Magnesium Sulfate Injection, USP, 50% due to the presence of glass particulate matter.
Product
Magnesium Sulfate Injection, USP, 50% (25 grams/50 mL), For IM or IV Use, 50 mL, Single Dose Vial, Rx only, Preservative Free, APP Pharmaceuticals, LLC, Schaumburg, IL, 60173, NDC 63323-064-50
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Food)·F-1828-2013·2013-08-28
NuGo Dark Mocha Non-Dairy Coffee Creamer Recalled for Undeclared Milk
NuGo Nutrition HQ is recalling Dark Mocha Non-Dairy coffee creamer because it may contain undeclared milk, posing a risk to people with milk allergies.
Product
NuGo Dark Mocha, 1.59 oz (45g) Non-Dairy
Category
Food
Distribution
Distributed nationwide
CriticalFDA (Food)·F-1830-2013·2013-08-28
NuGo Dark Peanut Butter Cup Recalled for Undeclared Milk
NuGo Nutrition HQ is recalling Dark Peanut Butter Cups labeled as non-dairy because they may contain undeclared milk.
Product
NuGo Dark Peanut Butter Cup, 1.59 oz (45g) Non-Dairy
Category
Food
Distribution
Distributed nationwide
CriticalFDA (Food)·F-1834-2013·2013-08-28
Whole Foods Recalls Crave Brothers Les Freres Cheese for Listeria Risk
Whole Foods Market is recalling Crave Brothers Les Freres cheese due to potential Listeria monocytogenes contamination, which can cause serious infections in vulnerable populations.
Product
Crave Brothers Les Freres cheese sold with labeling as: Les Freres, Crave Brothers Les Freres, Les Freres Wash Rind Product of USA, Crave Bros Les Freres, Crave Brothers Les Freres Cheese by Pound, Les Freres Crave Brothers, and Les Freres Crave Brothers PO-RK. Cheese was cut…
Category
Food
Distribution
Distributed nationwide
CriticalFDA (Food)·F-1833-2013·2013-08-28
NuGo Slim Espresso Recalled for Undeclared Milk Allergen
NuGo Nutrition HQ is recalling NuGo Slim Espresso Non-Dairy products because they may contain undeclared milk. Consumers with milk allergies should not consume the product.
Product
NuGo Slim Espresso, 1.59 oz (45g) Non-Dairy
Category
Food
Distribution
Distributed nationwide
CriticalFDA (Food)·F-1809-2013·2013-08-21
Crave Brothers Farmstead Cheese Recalled Due to Listeria Investigation
Crave Brothers Farmstead Cheese is recalling specialty cheese products while regulatory agencies investigate a potential Listeria monocytogenes contamination.
Product
Crave Brothers Farmstead Classics Les Freres Semi-Soft French Style Cheese, LF225. 2.5 lb wheel packaged in cheese paper. Two 2.5 lbs wheels in a case.
Category
Food
Distribution
9 states
CriticalFDA (Food)·F-1810-2013·2013-08-21
Crave Brothers Petit Frere Cheese Recalled Due to Listeria Investigation
Crave Brothers Farmstead Cheese is recalling Petit Frere Soft Ripened Cheese because of a multi-state Listeria monocytogenes investigation.
Product
Crave Brothers Farmstead Classics Petit Frere Soft Ripened Cheese, PF88. Net Wt. 8 oz. (227g). Packaged in cheese paper and sold inside a wooden box. Eight 8 oz wheels per case.
Category
Food
Distribution
9 states
CriticalFDA (Food)·F-1807-2013·2013-08-21
Gold Star Herring Fillets Recalled for Listeria Contamination
Gold Star Smoked Fish Corp. is recalling RYBACKA WIES brand Herring Fillets in Oil due to Listeria monocytogenes contamination found by New York State sampling.
Product
RYBACKA WIES brand HERRING FILLETS IN OIL (MATJES SLEDZ W OLEJU), Net Wt. 17.6 oz. (500g), UPC 0 21143 24122 8, Distributed By Gold Star, Inc., Brooklyn, NY 11231 --- The product is vacuum packed in a sealed plastic package.
Category
Food
Distribution
11 states

How to read this listing

Filters

6251–6275 of 7452