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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36251–36275 of 39777

  • CriticalFDA (Food)·F-0015-2013·2012-10-10

    Taylor Farms Recalls Wawa Mangoes Due to Salmonella Risk

    Taylor Farms is recalling Wawa mangoes because they may contain Daniella Brand mangoes contaminated with Salmonella Braenderup.

    Product
    Wawa Mango Net Wt. 8 oz (227 g) Distributed by Wawa, Inc. Wawa, PA 19063 UPC 726191069267
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Food)·F-0019-2013·2012-10-10

    Taylor Farms Recalls Wawa Mixed Fruit Due to Salmonella Risk

    Taylor Farms is recalling Wawa mixed fruit trays because they may contain mangoes contaminated with Salmonella Braenderup.

    Product
    Wawa Large mixed fruit Net Wt 12 oz (340 g) in rigid plastic trays Distributed by: Wawa, Inc. Wawa, PA 19063 UPC 726191069250. Wawa Small mixed fruit Net Wt 7.5 oz (213 g) in rigid plastic trays Distributed by: Wawa, Inc. Wawa, PA 19063 UPC 726191069243
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Food)·F-0017-2013·2012-10-10

    Taylor Farms Recalls Wawa Pineapple Due to Salmonella Risk

    Taylor Farms is recalling Wawa pineapple trays because they may contain mangoes contaminated with Salmonella Braenderup or were processed on shared equipment.

    Product
    Wawa pineapple Net Wt. 7 oz (198 g) rigid plastic tray Distributed by: Wawa, Inc. Wawa, PA 19063 UPC 726191069328
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Food)·F-0014-2013·2012-10-10

    DFI Cantaloupes Recalled Due to Salmonella Contamination

    DFI Marketing Inc. is recalling cantaloupes found positive for Salmonella by USDA testing. The affected melons were distributed nationwide and to Mexico.

    Product
    Cantaloupes are packed in 6ct, 9ct, 12ct, 15ct, 18ct, cardboard cartons with the DFI Brand. "826 California Westside" is also stamped on outside of the carton. Each cantaloupe also has a DFI brand sticker on it.
    Category
    Food
    Distribution
    21 states
  • SevereFDA (Food)·F-2440-2012·2012-10-10

    Sadie's Salads Potato Salad Recalled for Undeclared Allergens

    Sadie's Salads is recalling Red Skin Potato Salad tubs because the labels fail to declare eggs, milk, and soybean oil.

    Product
    Sadie's Salads Red Skin Potato Salad, 5 lb, 10 lb and 30 lb plastic tubs
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Devices)·Z-2478-2012·2012-10-10

    Zimmer Recalls VerSys Provisional Femoral Heads Due to Fit Issues

    Zimmer, Inc. is recalling VerSys provisional femoral heads because complaints report sub-optimal fit with mating components, leading to intraoperative dislodging.

    Product
    12/14 Neck Taper 00789504001 VerSys Femoral Head Provisional 40mm -3.5 00789504002 VerSys Femoral Head Provisional 40mm +0 00789504003 VerSys Femoral Head Provisional 40mm +3.5 00789504004 VerSys Femoral Head Provisional 40mm +7 00789504005 VerSys Femoral Head Provisional…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2474-2012·2012-10-10

    Zimmer Recalls VerSys Provisional Femoral Heads Due to Fit Issues

    Zimmer, Inc. is recalling VerSys provisional femoral heads because they may fit too loosely or too tightly with mating components, posing a risk of intraoperative dislodging.

    Product
    00789502601 VerSys Femoral Head Provisional 26mm -3.5 00789502602 VerSys Femoral Head Provisional 26mm +0 00789502603 VerSys Femoral Head Provisional 26mm +3.5 00789502604 VerSys Femoral Head Provisional 26mm +7 00789502605 VerSys Femoral Head Provisional 26mm +10.5 12/14…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2484-2012·2012-10-10

    Zimmer Recalls Provisional Femoral Heads Due to Fit Issues

    Zimmer, Inc. is recalling provisional femoral heads used in hip surgery due to reports of sub-optimal fit with mating components.

    Product
    00780304001 MIS 12/14 Slotted Femoral Head Provisional -3.5X36 00780304002 MIS 12/14 Slotted Femoral Head Provisional +0X36 00780304003 MIS 12/14 Slotted Femoral Head Provisional +3.5X36 00780304004 MIS 12/14 Slotted Femoral Head Provisional +7X36 00780304005 MIS 12/14…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0011-2013·2012-10-10

    Coast Tropical Brand Whole Mangoes Recalled for Salmonella Risk

    Coast Citrus Dist is recalling 2,630,663 boxes of Coast Tropical Brand Whole Mangoes due to potential Salmonella Branderup contamination.

    Product
    Coast Tropical Brand Whole Mangoes, Kent & Keitt's varieties, 10 lb box. The recalled mangos were sold between July 7, and August 30, 2012 and can be identified by the brand sticker along with one of the following numbers: 3114, 4051, 4311, 4584, and 4959 and the words…
    Category
    Food
    Distribution
    22 states
  • SevereFDA (Devices)·Z-2473-2012·2012-10-10

    Zimmer Recalls VerSys Provisional Femoral Heads Due to Fit Issues

    Zimmer, Inc. is recalling VerSys provisional femoral heads because they may fit too loosely or too tightly with mating components, posing a risk of intraoperative dislodging.

    Product
    00789502202 VerSys Femoral Head Provisional 22mm +0 00789502203 VerSys Femoral Head Provisional 22mm +3.5 00789502220 VerSys Femoral Head Provisional 22mm -2 00789502230 VerSys Femoral Head Provisional 22mm +3 12/14 Neck Taper The provisional heads replicate final femoral…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2482-2012·2012-10-10

    Zimmer Recalls Provisional Femoral Heads Due to Fit Issues

    Zimmer, Inc. is recalling provisional femoral heads used in hip surgery due to reports of sub-optimal fit with mating components.

    Product
    00780303201 MIS 12/14 Slotted Femoral Head Provisional -3.5X32 00780303202 MIS 12/14 Slotted Femoral Head Provisional +0X32 00780303203 MIS 12/14 Slotted Femoral Head Provisional +3.5X32 00780303204 MIS 12/14 Slotted Femoral Head Provisional +7X32 00780303205 MIS 12/14…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0012-2013·2012-10-10

    Dole Sliced Mushrooms Recalled for Potential Listeria Contamination

    Oakshire Mushroom Sales is recalling Dole brand sliced mushrooms due to potential Listeria monocytogenes contamination. The product was distributed to Albertson's.

    Product
    Dole brand Sliced Mushrooms, Net Wt. 8 OZ. (227G), UPC: 0 33383 67600 5, in a plastic container over-wrapped with plastic film. Labeled in part: Dole Sliced Mushrooms, Distributed by Oakshire Mushroom Sales, LLC under license Kennett Square, PA 19348 1-866-355-2077, Product…
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·F-0013-2013·2012-10-10

    Spokane Produce Recalls Champ's Sliced White Mushrooms for Listeria Risk

    Spokane Produce, Inc. is recalling Champ's Sliced White Mushrooms due to potential contamination with Listeria monocytogenes. The product was distributed in six states and to military bases.

    Product
    Champ's Sliced White Mushrooms, 227 g/8 oz, in a styrofoam container with shrink wrap, UPC 0 33383 67600 5. Labeled in part: "CHAMP'S MUSHROOMS Sliced White Mushrooms, Product of Canada, 227g/8 oz, 0 33383 67600 5 KEEP REFRIGERATED
    Category
    Food
    Distribution
    5 states
  • SevereFDA (Devices)·Z-2477-2012·2012-10-10

    Zimmer Recalls VerSys Provisional Femoral Heads Due to Fit Issues

    Zimmer, Inc. is recalling VerSys provisional femoral heads because they may fit too loosely or too tightly with mating components, posing a risk of intraoperative dislodging.

    Product
    00789503601 VerSys Femoral Head Provisional 36mm -3.5 00789503602 VerSys Femoral Head Provisional 36mm +0 00789503603 VerSys Femoral Head Provisional 36mm +3.5 00789503604 VerSys Femoral Head Provisional 36mm +7 00789503605 VerSys Femoral Head Provisional 36mm +10.5 12/14…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2493-2012·2012-10-10

    Zimmer Recalls Cemented Tibial Drills Due to Bone Perforation Reports

    Zimmer, Inc. is recalling 60 Cemented Tibial Drills for the Persona Personalized Knee System after three reports of tibial cortex perforation during use.

    Product
    Cemented Tibial Drill Product Usage: The cemented tibial drill is used to prepare the tibial bone prior to the impaction of the applicable stemmed tibial broach. The cemented tibial drill has engraved lines that are size specific to guide the user as to the depth to insert…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2475-2012·2012-10-10

    Zimmer VerSys Provisional Femoral Heads Recalled for Fit Issues

    Zimmer, Inc. is recalling VerSys provisional femoral heads due to reports of sub-optimal fit with mating components, which can cause intraoperative dislodging.

    Product
    00789502801 VerSys Femoral Head Provisional 28mm -3.5 00789502802 VerSys Femoral Head Provisional 28mm +0 00789502803 VerSys Femoral Head Provisional 28mm +3.5 00789502804 VerSys Femoral Head Provisional 28mm +7 00789502805 VerSys Femoral Head Provisional 28mm +10.5 12/14…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2359-2012·2012-10-10

    Cucina Fresca Smoked Tomato Sauce Recalled for Undeclared Milk

    Cucina Fresca, Inc. is recalling Smoked Tomato Sauce because the jars contain a different product with undeclared milk, posing a risk to consumers with milk allergies.

    Product
    Cucina Fresca Smoked Tomato Sauce. Product is packaged in a glass jar, net weight 24 oz. The UPC is 8-84337 00522-4
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Food)·F-1072-2012·2012-10-10

    Sadie's Salads Broccoli Salad Recalled for Undeclared Allergens

    Sadie's Salads is recalling Broccoli Salad because the label fails to declare egg, milk, and soybean oil allergens.

    Product
    Sadie's Salads Broccoli Salad, 8 lb and 25 lb plastic tubs
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Devices)·Z-2480-2012·2012-10-10

    Zimmer Recalls MIS Slotted Femoral Head Provisional Medical Devices

    Zimmer, Inc. is recalling MIS 12/14 Slotted Femoral Head Provisional devices due to reports of sub-optimal fit with mating components, which can lead to intraoperative dislodging.

    Product
    00780302601 MIS 12/14 Slotted Femoral Head Provisional -3.5X26 00780302602 MIS 12/14 Slotted Femoral Head Provisional +0X26 00780302603 MIS 12/14 Slotted Femoral Head Provisional +3.5X26 00780302604 MIS 12/14 Slotted Femoral Head Provisional +7X26 00780302605 MIS 12/14…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2476-2012·2012-10-10

    Zimmer Recalls VerSys Provisional Femoral Heads Due to Fit Issues

    Zimmer, Inc. is recalling VerSys provisional femoral heads because they may fit too loosely or too tightly with mating components, posing a risk of intraoperative dislodging.

    Product
    12/14 Neck Taper 00789503201 VerSys Femoral Head Provisional 32mm -3.5 00789503202 VerSys Femoral Head Provisional 32mm +0 00789503203 VerSys Femoral Head Provisional 32mm +3.5 00789503204 VerSys Femoral Head Provisional 32mm +7 00789503205 VerSys Femoral Head Provisional…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0011-2013·2012-10-10

    Philips HeartStart XL Defibrillators Recalled for Battery Failure Risk

    Philips is recalling HeartStart XL Defibrillators used with specific M3516A batteries that may fail without warning, potentially causing the device to shut down unexpectedly during use.

    Product
    Philips HeartStart XL M4735A Defibrillator/Monitors, used with the M3516A batteries The Heart Start XL Defibrillator/Monitor is a fully featured, defibrillator intended for use by qualified medical personnel, trained in either Advanced Cardiac Life Support or in the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2481-2012·2012-10-10

    Zimmer Recalls Provisional Femoral Heads Due to Fit Issues

    Zimmer, Inc. is recalling MIS and VerSys provisional femoral heads due to reports of sub-optimal fit with mating components, which can lead to intraoperative dislodging.

    Product
    00780302801 MIS 12/14 Slotted Femoral Head Provisional -3.5X28 00780302802 MIS 12/14 Slotted Femoral Head Provisional +0X28 00780302803 MIS 12/14 Slotted Femoral Head Provisional +3.5X28 00780302804 MIS 12/14 Slotted Femoral Head Provisional +7X28 00780302805 MIS 12/14…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2483-2012·2012-10-10

    Zimmer Recalls Provisional Femoral Heads Due to Fit Issues

    Zimmer, Inc. is recalling MIS 12/14 Slotted Femoral Head Provisional devices because they may fit too loosely or too tightly with mating components.

    Product
    00780303601 MIS 12/14 Slotted Femoral Head Provisional -3.5X36 00780303602 MIS 12/14 Slotted Femoral Head Provisional +0X36 00780303603 MIS 12/14 Slotted Femoral Head Provisional +3.5X36 00780303604 MIS 12/14 Slotted Femoral Head Provisional +7X36 00780303605 MIS 12/14…
    Category
    Medical Device
    Distribution
    Distributed nationwide