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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24051–24075 of 90112

  • HighNHTSA·22V617000·2022-08-11

    Third-Row Seat Belt Buckle Rivet Defect in 2021-2022 GMC Yukon and Related Vehicles

    General Motors is recalling 484,155 vehicles with improperly formed rivets on third-row seat belt buckle assemblies. The defect may prevent proper seat belt restraint in a crash, increasing injury risk.

    Product
    CADILLAC — CADILLAC, CHEVROLET, GMC ESCALADE, ESCALADE ESV, SUBURBAN, TAHOE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1513-2022·2022-08-10

    Pecan Deluxe Candy Double Fudge Blend recalled for undeclared peanut allergen

    Pecan Deluxe Candy Company is recalling Double Fudge Blend candy due to potential undeclared peanut content, which poses a risk to consumers with peanut allergies.

    Product
    Double Fudge Blend (04-3118-35) 35lbs. (15.88 KG) packaged in a blue plastic bag (ZZ500) inside a printed corrugated box (ZZ240),
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-1515-2022·2022-08-10

    FDA Recalls Vital Honey Supplement Containing Undeclared Tadalafil

    The FDA has recalled Dose Vital VIP Products Vital Honey With Caviar and Tongkat Ali Powder due to undeclared Tadalafil. The product was distributed in seven states and poses serious health risks.

    Product
    Dose Vital VIP Products Vital Honey With Caviar and Tongkat Ali Powder; 12 sachets-15g
    Category
    Food
    Distribution
    7 states
  • SevereFDA (Food)·F-1514-2022·2022-08-10

    Honey supplement recalled nationwide for undeclared sildenafil content

    Kingdom Honey Royal Honey VIP is recalled due to undeclared sildenafil, a pharmaceutical ingredient. The product was distributed nationwide; all lots are affected.

    Product
    Kingdom Honey Royal Honey VIP The Ultimate Power Source; 12 sachets-20g; UPC 555755 800036
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V614000·2022-08-10

    BMW Recalls 2018 540D xDrive Vehicles Due to EGR Module Fire Risk

    BMW is recalling 2018 540D xDrive vehicles because an internal leak in the EGR cooler may cause coolant to mix with soot, creating smoldering particles and a melting intake manifold that increases fire risk.

    Product
    BMW — BMW 540D
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1333-2022·2022-08-10

    SANGTER Energy Supplement Capsules Recalled for Undisclosed Sildenafil

    Distributor RFR, LLC is recalling SANGTER Energy Supplement Capsules because FDA analysis found they contain undisclosed sildenafil without FDA approval. The product was distributed nationwide and internationally.

    Product
    SANGTER Energy Supplement Capsules, 3000mg x 7 grain, 7-count blister pack within a carton, Distributed by: Distributor RFR, LLC, (800) 519-0204 Miami 33172 FL, USA; UPC 0 705632 523285
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1401-2022·2022-08-10

    SARS-CoV-2 Rapid Antigen Test Kits Distributed Without FDA Approval

    North American Diagnostics is recalling SARS-CoV-2 rapid antigen test kits that were distributed without FDA approval or clearance. Approximately 122,366 units were sold to consumers across multiple US states and internationally.

    Product
    SARS CoV 2 rapid antigen test kits packaged under the following brands: Oral Rapid Test, Oral Rapid Antigen Test, SML LDT Kits, SML Brand Finished Kits, SML Brand BT Test Kits, SML Brand BT Antigen Test Kit LDT
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1350-2022·2022-08-10

    SUSTANGO supplement capsules recalled for undisclosed tadalafil content

    SUSTANGO capsules contain the undisclosed pharmaceutical ingredient tadalafil and were marketed without FDA approval. Approximately 750 cartons were distributed nationwide via Amazon.

    Product
    SUSTANGO (Pendenadril Tytrate Blend) Capsules, 400 mg, 10-count blisters per carton, Formulated by: Male FX Labs, Bangor, ME, ASIN X0024468I9.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1482-2022·2022-08-10

    PRESTIGE RETRACTION GRASPER recalled due to potential weld separation

    The FDA is recalling 399 units of the PRESTIGE RETRACTION GRASPER surgical instrument due to risk of weld separation between the handle and shaft. This defect could cause device malfunction during surgical procedures.

    Product
    PRESTIGE RETRACTION GRASPER, W/PORT DUAL ACTION, ROTATING 5mm DIAM., 36cm LENGTH. Product Code 8361-10
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1498-2022·2022-08-10

    Atellica CH Iron_2 Diagnostic Device Produces False Microalbumin Results from Reagent Carryover

    Siemens Atellica CH Iron_2 in vitro diagnostic devices are being recalled because they produce falsely elevated microalbumin test results when a microalbumin test immediately follows an iron test. No illnesses have been reported.

    Product
    Atellica CH Iron_2 (Iron_2) is for in vitro diagnostic use in the quantitative determination of iron in human serum and (lithium heparin) plasma samples.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1303-2022·2022-08-10

    Matzim LA Extended-Release Tablets Recalled for Dissolution Specification Failure

    Matzim LA Extended-Release Tablets, 240 mg are being recalled due to failed dissolution specifications. Patients taking this medication should consult their doctor about their treatment.

    Product
    Matzim LA (Diltiazem Hydrochloride) Extended-Release Tablets, 240 mg, 30-count bottles, Rx Only, Manufactured by: Actavis Laboratories FL, Inc., Fort Lauderdale, FL USA 33314, USA, Distributed by: Actavis Pharma Inc., Parsippany, NJ 07054 USA; NDC 58544-692-30.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1537-2022·2022-08-10

    Vicks ZzzQuil Melatonin Syrup recalled for unapproved manufacturing process

    Procter & Gamble is recalling 90,522 cases of Vicks ZzzQuil Liquid Melatonin Syrup due to being an acidified/low-acid dietary supplement without an FDA-approved manufacturing process.

    Product
    Vicks ZzzQuil Liquid Melatonin Syrup Adult 8oz plastic bottle sold as single and twin pack
    Category
    Food
    Distribution
    45 states
  • HighFDA (Devices)·Z-1481-2022·2022-08-10

    Endoscopic Grasper Instruments Recalled Due to Weld Separation Risk

    Aesculap Implant Systems is recalling PRESTIGE ATRAUMATIC GRASPER surgical instruments because the weld connecting the handle to the shaft may separate during use.

    Product
    PRESTIGE ATRAUMATIC GRASPER W/PORT DUAL ACTION, ROTATING 5mm DIAM., 36cm LENGTH. Product Code 8360-10
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1530-2022·2022-08-10

    Grandpa's Yogurt Muffins Recalled Due to Temperature Abuse During Delivery

    United Natural Foods, Inc. is recalling Grandpa's brand yogurt muffins sold in Alabama and Mississippi due to temperature abuse during delivery to retail stores. No illnesses have been reported.

    Product
    NON-SHELF STABLE BAKED GOODS 1. GRANDPAS GRANDPAS ALMD PPY YGRT MFFN UPC 75563912378 5 OZ MORRISONS PASTRY COR 2. GRANDPAS GRANDPAS BRY BLST YGRT MFFN UPC 75563912363 5 OZ MORRISONS PASTRY COR 3. GRANDPAS GRANDPAS BB CRMB YGRT MFFN UPC…
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-1518-2022·2022-08-10

    Frozen deli salads recalled due to temperature abuse during delivery

    United Natural Foods, Inc. recalls frozen deli salads and prepared foods distributed in Alabama and Mississippi due to temperature abuse during delivery to retail stores.

    Product
    DELI SALADS 1. ASK ASK FOODS LOADED BAKED POTATO SALAD UPC 4742641052 5 LB ASK FOODS INC 2. ASK ASK FOODS SMOKEY MOZZARELLA PASTA SALAD UPC 4742650893 2 5 LB ASK FOODS INC 3. ASK ASK FOODS SMOKEY…
    Category
    Food
    Distribution
    2 states
  • HighFDA (Drugs)·D-1302-2022·2022-08-10

    Prescription Drug Matzim LA Extended-Release Tablets Recalled for Failed Dissolution

    Teva Pharmaceuticals is recalling Matzim LA (Diltiazem Hydrochloride) 180 mg tablets because they failed to meet dissolution specifications. The recall affects approximately 8,022 bottles distributed nationwide in the United States and Puerto Rico.

    Product
    MATZIM LA — MATZIM LA (DILTIAZEM HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·22V613000·2022-08-10

    Altec Recalls 2015-2022 Aerial Devices Due to Weld Crack Risk

    Altec Industries is recalling 2015-2022 DT65 and DT85 Aerial Devices because a weld crack could cause the auger bracket to detach, increasing injury risk.

    Product
    ALTEC — ALTEC AERIAL DEVICE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1535-2022·2022-08-10

    Vicks Children's Botanicals Liquid Nighttime Recalled for Improper Processing

    The Procter & Gamble Company is recalling Vicks Children's Botanicals Liquid Nighttime due to manufacturing without an approved acidification process. The product's preservation safety cannot be assured.

    Product
    Vicks Children's Botanicals Liquid Nighttime 4oz plastic bottle
    Category
    Drug
    Distribution
    45 states
  • HighFDA (Food)·F-1524-2022·2022-08-10

    Frozen Foods Recalled Due to Temperature Abuse During Delivery

    United Natural Foods, Inc. is recalling multiple brands of frozen prepared foods distributed to retail stores in Alabama and Mississippi due to temperature abuse during delivery. The temperature-abused foods may have been exposed to unsafe conditions allowing bacterial growth.

    Product
    FROZEN PREPARED FOODS 1. FRESH MARKET GLUTEN FREE COMBO PIZZA UPC 73709421202 12 OZ DI MANUFACTURING 2. FRESH MARKET GLUTEN FREE PEPPERONI PIZZA UPC 73709421016 12 OZ DI MANUFACTURING 3. FRESH MARKET GF MARGHRITA PIZZA…
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-1521-2022·2022-08-10

    Frozen Seafood Products Recalled Due to Temperature Abuse During Delivery

    Multiple frozen seafood products from various brands distributed in Alabama and Mississippi were recalled due to temperature abuse during delivery to retail stores. No illnesses have been reported.

    Product
    1. SPENCE SMOKED SALMON PINWHEELS 4 OZ UPC 76333600866 4 OZ ACME SMOKED FISH COR 2. ISABELLES HMSTYL TUNA SALAD UPC 71070840624 5LB SALAD BAR TENDERS 3. ISABELLES MD MACARONI SHRIMP SALAD 5 LB UPC 71070843184 5 LB…
    Category
    Food
    Distribution
    2 states
  • HighFDA (Devices)·Z-1484-2022·2022-08-10

    E-100 Generator electrosurgical units recalled due to preventative maintenance oversight

    Intuitive Surgical is recalling 505 E-100 electrosurgical generators because required preventative maintenance was not performed on units distributed worldwide and in the US.

    Product
    The E-100 Generator (PN 374848-09) is a bipolar electrosurgical unit (ESU) designed to be used with the da Vinci Xi and X systems. The E-100 is installed on the Vision Cart and is connected to the system. The functions of the E-100 are initiated by the foot pedals on the Surgeon…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1516-2022·2022-08-10

    Ragozzino Foods Creamy Parmesan Risotto Recalled for Glass Contamination

    Ragozzino Foods is recalling Creamy Parmesan Risotto distributed in New York, Florida, Illinois, and California due to potential glass contamination. Consumers should not eat the affected product.

    Product
    Creamy Parmesan Risotto; Net Weight: 24 lbs (6/64oz pouches); Manufactured by: Ragozzino Foods, Inc. Meridien, CT
    Category
    Food
    Distribution
    4 states
  • HighFDA (Food)·F-1526-2022·2022-08-10

    Multiple brands of frozen vegetables recalled for temperature abuse during delivery

    United Natural Foods, Inc. is recalling multiple brands of frozen vegetable products distributed in Alabama and Mississippi due to temperature abuse during delivery to retail stores.

    Product
    FROZEN VEGETABLE PRODUCTS 1. RESERS RESER CREAMY MASHED POTATOES UPC 7111714446 5LB RESERS FINE FOODS IN 2. SIMPLOT SIMPLOT ROASTED BABY BAKERS UPC 7117900048 2.5 LB J R SIMPLOT COMPANY 3. ALEXIA ALEXIA SWT POT WAFL FRIES UPC…
    Category
    Food
    Distribution
    2 states