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.
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 deaths or serious injuries are reported, 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.
Minimum severity
Kingdom Creamery of Vermont is recalling 14% Base Mix and Archie Case Mix ice cream base products due to Listeria monocytogenes contamination. A Class I FDA recall affects 1,623 cases distributed to Vermont, Maine, and Massachusetts.
HeartWare HVAD System Batteries are being recalled due to electrical faults that may prevent the battery from powering the device controller, accepting charges, or maintaining charge. Approximately 19,616 batteries distributed worldwide are affected.
Kingdom Creamery of Vermont is recalling 1,623 cases of 14% Chocolate Base Mix (Lot 220724, Best By Date 8/11/22) distributed in VT, ME, and MA due to potential Listeria monocytogenes contamination.
Kingdom Creamery of Vermont's 14% Base Mix is being recalled due to potential Listeria monocytogenes contamination. The product was distributed in Vermont, Maine, and Massachusetts.
Kabobs Acquisition Inc. is recalling Tomato, Basil & Mascarpone Arancini products due to possible glass contamination from their rice supplier. Affected lot numbers include PM22F23, PM22F30, and PM22G13.
Clearblue Smart Countdown pregnancy tests distributed to Family Dollar stores were not stored in temperature-controlled conditions. Consumers who purchased this product should return it for a refund or replacement.
FACTOR is recalling Factor Vegan Mushroom Marsala 12.7oz meals due to glass contamination in the arborio rice ingredient. The recall affects 48,962 units with best-by dates in June and July 2022.
Trinity Sterile's Wolf Pak Premium Dressing Change Kit is mislabeled as latex-free but contains natural rubber latex in component 94-7002. This poses a risk to people with latex allergies.
Aire-Master of America is recalling Avant Foaming Hand Sanitizer due to a manufacturing process deviation where the deionized water system lacked proper microbial controls during production.
Baxter Healthcare recalls 85,680 bags of acetaminophen injection nationwide due to temperature abuse in distribution. Product was shipped in refrigerated trucks despite being labeled for room temperature storage.
Nephron Sterile Compounding Center is recalling PF-Labetalol HCl Injection nationwide due to manufacturing deviations that create potential for cross-contamination. No illnesses have been reported.
Factor is recalling its Caramelized Onion & Goat Cheese Risotto due to glass fragments in an arborio rice ingredient. The contamination poses a choking and injury risk.
Blue Diamond Growers is recalling whole brown almonds due to potential Salmonella contamination. Although none of the recalled products tested positive, the company is conducting a precautionary recall.
ASO LLC is recalling 274,458 retail packages of three wound care products that fall apart during handling after removal from packaging, compromising their sterility and usability.
Protect U Guard Foaming Hand Sanitizer is being recalled because it was manufactured with deionized water from a system lacking proper microbial controls. The affected product was distributed in Florida, Illinois, Iowa, and New Jersey.
Akorn, Inc. is recalling 14,712 bottles of PrednisoLONE Oral Solution (15 mg/5 mL) due to incomplete induction seals in containers. No illnesses have been reported, but the defect may affect product integrity.
Family Dollar is recalling Fixodent Org Cream denture adhesive (2.4oz and 0.75oz travel sizes) sold May-June 2022 due to improper storage in non-temperature-controlled areas. No illnesses reported.
Minn Dak Growers recalls Fancy Buckwheat Flour due to plastic foreign material contamination. Two lot numbers were distributed in Indiana; affected consumers should discard the product.
Micro Therapeutics is recalling Echelon-14 Micro Catheters because outer packaging was exposed to moisture during transport. The moisture exposure could compromise the sterility or function of the device.
Family Dollar's NEW SKIN Liquid Bandage was not stored in temperature-controlled conditions, potentially compromising product integrity. Affected units were sold nationwide during May through June 2022.
Myolyn Inc. is recalling the power electronic box subassembly for the MyoCycle MC-2 because internal mounting screws may come loose during shipping, creating a risk of electrical shock.
Kabobs Acquisition Inc. is recalling Truffle Arancini with Wild Mushrooms due to potential glass pieces in the rice. The product was distributed to multiple states.
Simply Saline Nasal Mist 3.1 oz sold at Family Dollar stores has been recalled due to improper temperature storage between May and June 2022. Consumers should return the product to their local Family Dollar store.
Becton Dickinson recalls 9,340 units of BD PhaSeal Y-Site Connectors (Catalog 515304) due to incorrect expiration dates printed on product labels that extend beyond the actual product expiration.
Nephron Sterile Compounding Center is recalling 294 bags of Trisodium Citrate 0.5% Solution IV bags due to potential cross-contamination from manufacturing deviations. The affected lots were distributed nationwide.