The Recall Desk

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.

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20526–20550 of 39660

  • SevereFDA (Drugs)·D-0731-2017·2017-05-24

    Key Pharmacy Recalls PGE1 Injection Due to Sterility Concerns

    Key Pharmacy and Compounding Center is recalling PGE1 MDV 20mcg/mL injections due to a lack of assurance of sterility. The affected products were distributed in the U.S., Australia, and Canada.

    Product
    PGE1 MDV 20MCG/ML INJ, Injection, 20mcg/mL, Rx only, packaged in a 5 mL, 10mL, and 15 mL Glass/Multiple Dose vials, Prepared by Key Compounding Pharmacy
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2238-2017·2017-05-24

    Whole Foods Organic Vanilla Yogurt Parfait Cups Recalled for Undeclared Almonds

    Whole Foods is recalling single-serve Organic Vanilla Yogurt parfait cups with strawberries and granola because they contain undeclared almonds.

    Product
    Whole Foods single-serve Organic Vanilla Yogurt parfait cups with Strawberries and Granola, Various weights PLU 58260
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Drugs)·D-0760-2017·2017-05-24

    FDA Recalls Compounded Injection Due to Lack of Sterility Assurance

    Key Pharmacy and Compounding Center is recalling CHOL/IN/ME(L)/B6 10ML MDV injection due to lack of assurance of sterility.

    Product
    CHOL/IN/ME(L)/B6 10ML MDV 50/50/25/0.1MG/ML INJ, Injection, 50mg/50mg/25mg/0.1mg/mL, Rx only, 10mL Glass/Multiple Dose vial, Prepared by Key Compounding Pharmacy
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0716-2017·2017-05-24

    FDA Recalls Key Pharmacy Compounded Ferric Gluconate Injection for Sterility Concerns

    Key Pharmacy and Compounding Center is recalling a specific lot of compounded ferric gluconate injection due to a lack of assurance of sterility.

    Product
    FERR GLUC/PROCAINE 10ML MDV 60/10MG/ML INJ, Injection, 60mg/10mg/mL, Rx only, 10 mL glass/Multiple Dose vial, Prepared by Key Compounding Pharmacy
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0718-2017·2017-05-24

    Key Pharmacy Recalls Folinic Acid Injections Due to Sterility Concerns

    Key Pharmacy and Compounding Center is recalling specific lots of Folinic Acid injections because the firm cannot guarantee the products are sterile.

    Product
    FOLINIC ACID MDV (CALIF) 5MG/ML INJ, Injection, 5mg/mL, Rx only, packaged in 5 mL and10 mL glass/ Multiple Dose vial, Prepared by Key Compounding Pharmacy
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0775-2017·2017-05-24

    FDA Recalls Compounded Progesterone Injection Due to Sterility Concerns

    Key Pharmacy and Compounding Center is recalling compounded progesterone injections because the firm cannot ensure the products are sterile.

    Product
    PROGESTERONE SESAME OIL 10ML MDV 100MG/ML INJ, Injection, 100mg/mL, Rx only, 10mL Glass; Multiple Dose vial, Prepared by Key Compounding Pharmacy
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0786-2017·2017-05-24

    Key Pharmacy Recalls Vitamin D3 Injection Due to Sterility Concerns

    Key Pharmacy and Compounding Center is recalling specific lots of Vitamin D3 in Olive Oil Injection due to a lack of assurance of sterility.

    Product
    VITAMIN D3 IN OLIVE OIL SDV 100,000U/ML INJ, Injection, 150,000u/mL, Rx only, packaged in 2mL Glass/Single Dose vial, Prepared by Key Compounding Pharmacy
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0728-2017·2017-05-24

    Key Pharmacy Recalls Hydroxo-B12 Injections Due to Sterility Concerns

    Key Pharmacy and Compounding Center is recalling specific lots of Hydroxo-B12 injections because the firm cannot guarantee the products are sterile.

    Product
    HYDROXO-B12 5ML PBF MDV (CALIF) 10MG/ML INJ, Injection, 10mg/mL, RX only, 5mL Glass/Multiple Dose vial, Prepared by Key Compounding Pharmacy
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V331000·2017-05-22

    Ford Recalls 2015-2017 F-Series Trucks for Door Handle Cover Defect

    Ford is recalling specific 2015-2017 F-Series trucks equipped with chrome door handle covers that may cause doors to unlatch in a side impact, increasing injury risk.

    Product
    FORD — FORD F-150, redundant F-350, F-550, redundant F-250
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V332000·2017-05-22

    Ford Recalls 2017 Models for Manual Seat Recliner Weld Defect

    Ford is recalling 2017 Explorer and F-Series trucks because manual seat back recliners may have inadequate welds, increasing injury risk in a crash.

    Product
    FORD — FORD EXPLORER, F-150, F-550 SD, F-350 SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalCPSC·17159·2017-05-19

    Blomberg and Summit Electric Ranges Recalled for Electrocution Hazard

    Arçelik A.S. is recalling about 6,300 Blomberg and Summit electric ranges because they can become energized, posing shock and electrocution risks.

    Product
    Blomberg and Summit electric ranges
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V330000·2017-05-19

    Columbia Aliner Ascape Trailers Recalled for Loose Propane Gas Trays

    Columbia Northwest is recalling 2017-2018 Aliner Ascape trailers because liquid propane gas bottle trays may detach, increasing the risk of fire or crash.

    Product
    COLUMBIA — COLUMBIA ALINER ASCAPE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·051-2017·2017-05-18

    Osso Good Co. Recalls Beef and Pork Bone Broth Products

    The Osso Good Co. is recalling approximately 1,210 pounds of beef and pork bone broth products produced without federal inspection.

    Product
    Yosemite Protein Products, Inc. — The Osso Good Co. Recalls Beef and Pork Products Produced Without Benefit of Inspection
    Category
    Food
    Distribution
    5 states
  • SevereNHTSA·17V328000·2017-05-18

    BMW Recalls 2005-2008 7 Series Vehicles for Door Latch Defect

    BMW is recalling 2005-2008 7 Series and B7 Alpina vehicles because doors may appear latched but can unexpectedly open, risking occupant ejection.

    Product
    BMW — BMW 760LI, 750LI, 745I, 760I
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-2216-2017·2017-05-17

    Frito-Lay Recalls Miss Vickies Multipacks Due to Potential Salmonella

    Frito-Lay is recalling 32-count Miss Vickies Multipacks due to potential Salmonella contamination. The recall covers units distributed nationwide and in Puerto Rico.

    Product
    32 count Miss Vickies Multipack Box 44 oz. packaged in flexible plastic
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-2215-2017·2017-05-17

    Frito-Lay Recalls Lays Kettle Cooked Multipacks Due to Salmonella Risk

    Frito-Lay is recalling 1,196,880 units of Lays Kettle Cooked Multipack Trays nationwide due to the potential presence of Salmonella.

    Product
    30 count Lays Kettle Cooked Multipack Tray 41.25 oz. packaged in flexible plastic
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-2213-2017·2017-05-17

    Frito-Lay Bold Mix Sack Recalled for Potential Salmonella Presence

    Frito-Lay is recalling 20-count Bold Mix Sacks nationwide due to the potential presence of Salmonella.

    Product
    20 count Frito-Lay Bold Mix Sack 18.4 oz. packaged in flexible plastic
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2186-2017·2017-05-17

    Jimmy's Cookies Peanut Butter Chocolate Chunk Cookies Recalled for Undeclared Milk

    Jimmy's Cookies is recalling The Bakery Peanut Butter Chocolate Chunk Cookies because they may contain undeclared milk. The product was distributed nationwide.

    Product
    The Bakery Peanut Butter Chocolate Chunk Cookies, Net Wt. 14 oz. (396g), packaged in a clear plastic clam shell, UPC 0 78742 06652 3, Distributed by: Wal-Mart Stores, Inc. Bentonville, AR 72716
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2211-2017·2017-05-17

    Frito-Lay Recalls Jalapeño Flavored Potato Chips Due to Salmonella Risk

    Frito-Lay is recalling Jalapeño Flavored Lays Kettle Cooked and Miss Vickies Kettle Cooked potato chips due to a potential presence of Salmonella.

    Product
    Jalape¿o Flavored Lays Kettle Cooked potato chips and Jalape¿o Flavored Miss Vickies Kettle Cooked potato chips in the following unit sizes: 1.75 oz, 2.75 oz, 8 oz, 13.5 oz, 2.125 oz, 6.5 oz, 0.85 oz, 1.375 oz, 2.25 oz, and 1.375 oz
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2214-2017·2017-05-17

    Frito-Lay Recalls Miss Vickies Multipack Trays Due to Potential Salmonella

    Frito-Lay is recalling 30-count Miss Vickies Multipack Trays nationwide and in Puerto Rico due to the potential presence of Salmonella.

    Product
    30 count Miss Vickies Multipack Tray 41.25 oz. packaged in flexible plastic
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2042-2017·2017-05-17

    Arthrex Recalls Anthrex PEEK SwiveLock SP Vented Anchors Due to Breakage

    Arthrex, Inc. is recalling specific Anthrex PEEK SwiveLock SP Vented anchors because some eyelets broke during insertion. The recall covers units distributed in the US and several international locations.

    Product
    Anthrex PEEK SwiveLock SP Vented, 5.5mm x 24.5 mm, Self-Punching
    Category
    Medical Device
    Distribution
    49 states
  • SevereFDA (Devices)·Z-2045-2017·2017-05-17

    Arthrex SpeedBridge Implant System Recalled for Broken Eyelets

    Arthrex is recalling specific SpeedBridge Implant Systems because some eyelets broke during insertion. The recall covers multiple batches distributed in the US and internationally.

    Product
    Anthrex SpeedBridge Implant System with BioComposite SwiveLock SP Vented, 5.5 mm x 24 mm
    Category
    Medical Device
    Distribution
    49 states
  • SevereFDA (Devices)·Z-2050-2017·2017-05-17

    Mederi Stretta Catheter Recalled Due to Sterility Compromise

    Mederi Therapeutics is recalling 1,458 Stretta Catheter kits because a breach in the sterile barrier package compromised sterility.

    Product
    Mederi Stretta Catheter and Accessory Kit, Sterile For Use with the MEDERI MDRF1 GENERATOR ONLY. Used in the treatment of gastroesophageal reflux disease (GERD). REF 175-5580
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V324000·2017-05-17

    Isuzu Recalls NPR and GMC Trucks Due to Stuck Accelerator Pedal

    Isuzu is recalling certain 2008-2009 and 2012-2013 NPR, NPR HD, and GMC W3500/W4500 trucks because the throttle pedal may get stuck, causing high speeds and crash risk.

    Product
    ISUZU — ISUZU, CHEVROLET, GMC NPR, W3500, W4500, NPR HD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2068-2017·2017-05-17

    Zimmer Biomet Recalls Regenerex Patella Implants Due to Peg Shearing

    Zimmer Biomet is recalling 8,154 Regenerex Series A Patella implants because the pegs may shear after surgery.

    Product
    Regenerex Patella RGX 3 PEG SER A PATELLA 28MM RGX 3 PEG SER A PATELLA 31MM RGX 3 PEG SER A PATELLA 34MM RGX 3 PEG SER A PATELLA 37MM Product Usage: The Regenerex Series A Patella can be used for any non-cemented resurfaced 3-peg patella application within the Vanguard…
    Category
    Medical Device
    Distribution
    Distributed nationwide