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

31801–31825 of 39756

SevereFDA (Food)·F-1546-2014·2014-03-05
The Cultured Kitchen Recalls Six Cashew Cheese Varieties Due to Salmonella Risk
The Cultured Kitchen is recalling six varieties of cashew cheese with expiry dates up to April 19, 2014, due to potential Salmonella contamination.
Product
The Cultured Kitchen Pesto or Basil Pesto Cashew Cheese; Processed raw at low temperatures to preserve minerals, enzymes and nutrients. Wheat, dairy, soy and gluten free. This product contains live active cultures Keep Refrigerated 8 oz., (226.8 grams) Plastic container…
Category
Food
Distribution
1 state
SevereFDA (Devices)·Z-1047-2014·2014-03-05
Medline Recalls Angio Pack #2 Surgical Kits Due to Coating Defect
Medline Industries is recalling 768 units of Angio Pack #2 surgical kits because a guidewire component has a potential for its coating to flake off.
Product
ANGIO PACK #2; REF: DYNJ39185; Packaged in Mexico by: Medline Industries, Inc., Mundelein, IL 60060; 1-800-Medline; www.medline.com Surgical kit used to supply tools required to perform angiography medical procedures.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0953-2014·2014-03-05
Teleflex ISIS HVT Tracheal Tubes Recalled for Kinking Risk
Teleflex Medical is recalling ISIS HVT Tracheal Tubes because they can kink during patient use, potentially compromising the airway.
Product
ISIS HVT Tracheal Tube Cuffed with Subglottic Secretion Suction Port, 7.5, Rx only, Product Usage: A tracheal tube is a device inserted into a patients trachea via the nose or mouth and used to maintain an open airway.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-1545-2014·2014-03-05
The Cultured Kitchen Recalls Cashew Cheese for Salmonella Risk
The Cultured Kitchen is recalling six varieties of cashew cheese due to potential Salmonella contamination. Affected products have expiry dates up to and including April 19, 2014.
Product
The Cultured Kitchen Habanero Cilantro Lime Cashew Cheese; Processed raw at low temperatures to preserve minerals, enzymes and nutrients. Wheat, dairy, soy and gluten free. This product contains live active cultures Keep Refrigerated 8 oz., (226.8 grams) Plastic container…
Category
Food
Distribution
1 state
SevereFDA (Devices)·Z-0959-2014·2014-03-05
Teleflex ISIS HVT Tracheal Tubes Recalled for Kinking Risk
Teleflex Medical is recalling ISIS HVT Tracheal Tubes because they can kink during patient use, potentially compromising the airway.
Product
ISIS HVT Tracheal Tube Cuffed with Subglottic Secretion Suction Port and Preloaded Stylet, 7.0, Rx only, Product Usage: A tracheal tube is a device inserted into a patients trachea via the nose or mouth and used to maintain an open airway.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0961-2014·2014-03-05
Teleflex Recalls ISIS HVT Tracheal Tubes Due to Kinking Risk
Teleflex Medical is recalling specific lots of ISIS HVT Tracheal Tubes because they can kink during patient use, potentially compromising airway maintenance.
Product
ISIS HVT Tracheal Tube Cuffed with Subglottic Secretion Suction Port and Preloaded Stylet, 8.0, Rx only, Product Usage: A tracheal tube is a device inserted into a patients trachea via the nose or mouth and used to maintain an open airway.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1070-2014·2014-03-05
GE Healthcare Recalls Infant Resuscitation Systems Due to Reversed Fittings
GE Healthcare is recalling Giraffe and Panda infant resuscitation systems because oxygen and air inlet fittings were reversed during assembly.
Product
GE Healthcare - Giraffe Warmer;Panda Warmer;Panda iRes Warmer, Giraffe Stand-alone Infant Resuscitation System. Product Usage: The T-Piece Resuscitation System [ventilator, emergency powered resuscitator]/Panda Bag and Mask Resuscitation System provides the basic equipment…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1105-2014·2014-03-05
Fresenius Recalls Optiflux B200 Flux Dialyzers Due to Port Leak Risk
Fresenius Medical Care is recalling 100,008 Optiflux B200 Flux Dialyzers because the dialysate port may leak during priming.
Product
Optiflux B200 Flux Dialyzers; Product Number: 0500325E. Single Use acute or chronic hemanalysis treatment.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1077-2014·2014-03-05
DePuy PFC SIGMA Knee Implant Recall Due to Microstructure Defects
DePuy Orthopaedics is recalling PFC SIGMA knee implants with anomalous microstructure that may decrease fatigue strength and cause fracture.
Product
PFC SIGMA Cruciate Retaining (CR); Cemented Femoral devices; (Size 5/RT) Used during primary total knee arthroplasty to improve patient mobility.
Category
Medical Device
Distribution
4 states
SevereFDA (Food)·F-1556-2014·2014-03-05
Unified Grogers Recalls Ginger Snap Cookies for Undeclared Egg
Unified Grocers is recalling 12 oz. Ginger Snap Cookies because they contain undeclared egg. The recall affects products distributed in California, Arizona, and Nevada.
Product
Ginger Snap Cookies, 12 oz., Item Code: 48918, UPC 0-41380-23359
Category
Food
Distribution
3 states
SevereFDA (Food)·F-1547-2014·2014-03-05
The Cultured Kitchen Recalls White Cheddar Cashew Cheese for Salmonella Risk
The Cultured Kitchen is recalling White Cheddar Cashew Cheese due to potential Salmonella contamination. Affected products have expiry dates up to and including 4/19/2014.
Product
The Cultured Kitchen White Cheddar Cashew Cheese; Processed raw at low temperatures to preserve minerals, enzymes and nutrients. Wheat, dairy, soy and gluten free. This product contains live active cultures Keep Refrigerated 8 oz., (226.8 grams) Plastic container UPC…
Category
Food
Distribution
1 state
SevereFDA (Devices)·Z-1052-2014·2014-03-05
Medline Recalls Surgical Kits with Potential Coating Defect on Guidewires
Medline Industries is recalling 10 surgical kits containing guidewires with a potential coating defect. The kits were distributed to specific US states.
Product
STERILE SAMPLE BUILD; REF: SAMP0144; Packaged for Medline Industries, Inc., Mundelein, IL 60060; 1-800-Medline; www.medline.com Surgical kit used to supply tools required to perform medical procedures..
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·14V087000·2014-03-04
New Flyer Transit Buses Recalled for Potential Exhaust Fire Risk
New Flyer is recalling certain transit buses because condensation in the intake manifold may freeze, causing sensor issues that could lead to exhaust flames or vehicle fires.
Product
NEW FLYER — NEW FLYER C40LF, C40LFR, C35LF, C35LFR
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·14V095000·2014-03-04
Prevost Recalls 2013-2014 Coaches Due to Battery Cable Insulation Defect
Prevost is recalling 59 model year 2013-2014 coaches because defective battery cable insulation may cause the engine to shut down, increasing crash risk.
Product
PREVOST — PREVOST H3-45 VIP, H3-45, H3-41
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·14V097000·2014-03-04
Ford E-Series CNG Conversion Recall for Rear Cylinder Bracket Failure
Landi Renzo USA is recalling 2011-2014 Ford E-150, E-250, and E-350 vans modified for CNG because rear cylinder brackets may fail, risking a gas leak and fire.
Product
FORD — FORD E-350, E-150, E-250
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·14V103000·2014-03-04
Fiat 500L Recall: Transmission Shifter May Fail to Shift Gears
Chrysler is recalling 2014 Fiat 500L vehicles because the transmission shifter may not respond to driver input, potentially causing unintended vehicle movement.
Product
FIAT — FIAT 500L
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·14V085000·2014-02-28
MCI Recalls 2011-2012 D4000 Motorcoaches Due to Fire Risk
Motor Coach Industries is recalling 2011-2012 D4000 motorcoaches because condensation in the intake manifold may freeze, causing sensor failure that leads to exhaust flames or vehicle fire.
Product
MCI — MCI D4000
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·14V083000·2014-02-27
Blue Bird Recalls School Buses Due to Exhaust Fire Risk
Blue Bird is recalling 2009-2015 All American school buses because condensation in the intake manifold may freeze, causing elevated exhaust temperatures or flames that increase the risk of fire or burn injury.
Product
BLUE BIRD — BLUE BIRD ALL AMERICAN
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·14V084000·2014-02-27
Gillig Low Floor Transit Bus Recall for Engine Fire Risk
Gillig is recalling 2010-2014 Low Floor transit buses because condensation in the intake manifold may freeze, causing sensor failure and increasing the risk of a vehicle fire.
Product
GILLIG — GILLIG LOW FLOOR
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0980-2014·2014-02-26
Merit Medical Recalls Custom Procedural Trays Contaminated with Particulate Matter
Merit Medical Systems is recalling custom procedural trays containing 1% Lidocaine HCl injection due to visible particulate matter found in the product container.
Product
Merit Medical's Custom Procedural Trays or Kits containing 1% Lidocaine HCl Injection, USP, 10 mg/mL, Lot 25-090-DK. Custom Procedural Tray or kit is a combination of legally marketed medical devices placed into one container for the convenience of the user and used within the…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-1535-2014·2014-02-26
Kinnikinnick Gluten-Free Waffles Recalled for Undeclared Milk Allergen
DPI Specialty Foods is recalling Kinnikinnick gluten-free waffles because they may contain undeclared milk, despite labeling indicating the product is dairy-free.
Product
Kinnikinnick Gluten Free Original Homestyle Waffles Frozen Contains a logos on the package indicating it is gluten free, dairy free, and nut free. 210 g/7.4oz Qty/pkg - 6. UPC 62013300198 1. DPI item # 55844.
Category
Food
Distribution
2 states
SevereUSDA FSIS·017-2014·2014-02-26
Sun Hing Foods Recalls Canadian Liver Pâté Produced Without Inspection
Sun Hing Foods is recalling 1,282 pounds of Canadian liver pâté and spread that were not inspected by USDA at the U.S. border.
Product
California Firm Recalls Canadian Liver P,tE Products Produced Without Import Inspection
Category
Food
Distribution
13 states
SevereFDA (Food)·F-1536-2014·2014-02-26
StemVida Recalls StemAlive Capsules Due to Undeclared Milk Allergen
StemVida International is recalling StemAlive 90 Capsules because the product contains undeclared milk, a major food allergen.
Product
STEMALIVE, 90 Capsules. The product is in a white plastic bottle with white lid, the brand is StemVida International with a white and gold label. Product labeling reads in part:"STEMVIDA INTERNATIONAL***StemAlive***PROMOTES ADULT STEM CELL FUNCTION AND HEALTH***Dietary…
Category
Food
Distribution
10 states
SevereFDA (Devices)·Z-0995-2014·2014-02-26
Medtronic Recalls Select 3D Arterial Cannulae Due to Body Splitting
Medtronic is recalling Select 3D Arterial Cannulae because the device body may split near the suture collar.
Product
Medtronic Select 3D Arterial Cannulae. Vented, models 78618 (18 Fr.) and 78620 (20 Fr.). Non-Vented Cannulae, models 78718 (18 Fr.) and 78720 (20 Fr.). Sterilized using Ethylene Oxide. Non-pyrogenic. The Select 3D Arterial Cannulae both have clear flexible, thin wall…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1059-2014·2014-02-26
Elekta Synergy XVI Radiation Therapy System Recalled for Table Position Error
Elekta is recalling Synergy XVI radiation therapy systems because a software error can cause the treatment table to move to an incorrect position during specific online registration procedures.
Product
Synergy XVI XVI can incorrectly calculate the target position of the treatment table, because of an error that does not occur very frequently. This is the sequence of events when this error occurs - (1) You do an online VolumeView acquisition and registration. (2) You accept…
Category
Medical Device
Distribution
Distributed nationwide

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31801–31825 of 39756