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Rose and Shore frozen margarita thin crust pizza may contain metal pieces from contaminated tomatoes. The affected product was distributed to retailers in California, Oregon, Arizona, Idaho, and Texas. No injuries have been reported.

Moderate·FDA·Apr 1, 2026·Rose and Shore

Bakkavor recalled two bread products, Frederik's by Meijer Slow-Roasted Tomato & Shredded Parmesan focaccia and a Basil Pesto & Mozzarella pizza, because they may contain metal fragments. The company traced the problem to roasted tomatoes from one of its ingredient suppliers. The products were shipped to stores in AZ, CA, CT, FL, IL, MI, NC, NJ, TX and VA, and no injuries have been reported.

Moderate·FDA·Apr 1, 2026·Hello Fresh2 products

Sevillo Fine Foods is recalling frozen slow roasted diced tomatoes because they may contain metal fragments. The recall affects 24-lb bulk packages with specific lot numbers distributed in California and North Carolina.

Moderate·FDA·Apr 1, 2026·Sevillo Fine Foods2 products

Savannah Bee Company is recalling certain bottles of Honey BBQ Sauce labeled as "Mustard" because they actually contain the "Sweet" variety inside, which has undeclared soy and wheat allergens. The mislabeled bottles pose a serious risk to people with soy or wheat allergies. The affected product has UPC 8 50033 93758 9 and a best-before date of 05/16/27.

Moderate·FDA·Apr 1, 2026

American Laboratories is recalling three pepsin powder products because they may be contaminated with Salmonella. The products are Pepsin Full Strength Powder (50 kg), Pepsin 1:10,000 Powder (10 kg), and Pepsin 1:3000 Powder (50 kg), packed in cardboard drums or boxes and sold to wholesale accounts in several U.S. states and one account in Australia. No illnesses have been reported.

Moderate·FDA·Apr 1, 20263 products

Pacific Coast Fresh is recalling six King Harvest hummus varieties because they may contain aluminum pieces. The products are Jalapeno, Roasted Red Pepper, Sundried Tomato, Balsamic, Black Olive and Spinach Hummus, sold in 10 oz and 17 oz plastic tubs. They were distributed in Oregon and Washington, and no injuries have been reported.

Moderate·FDA·Apr 1, 2026·King Harvest6 products

Sunflour Bakery hamburger buns contain sesame seeds that are not listed on the package label. One 18-ounce bag (UPC 832971001522) with an expiration date of 02/24/2026 was distributed to a retailer in Orange County. People with sesame allergies could have a serious reaction if they eat these buns.

Moderate·FDA·Apr 1, 2026

Ajinomoto is recalling 11 fried rice and gyoza dumpling products because they may contain pieces of glass, 1 to 3 cm long and 2 to 4 mm wide. The products are sold under the Trader Joe's, Kroger, Ajinomoto, Ajinomoto Ling Ling, Tai Pei and Golden Tiger names and were distributed in 43 states. No injuries have been reported.

Moderate·FDA·Apr 1, 202611 products

Western Mixers is recalling two sizes of Chilli Spanish Peanuts because glass was found inside sealed containers. The products are sold under the First Street brand (11 oz containers) and the Treasured Harvest brand (25 lb bags). No injuries have been reported. The recall was sent to two businesses with a total of 53 retail locations nationwide.

Moderate·FDA·Apr 1, 20262 products

American Health Packaging is recalling specific batches of Meclizine Hydrochloride 12.5 mg tablets because they failed to meet required tablet specifications. The affected product is Lot #1024852 with an expiration date of 9/30/2026. No injuries have been reported.

Moderate·FDA·Apr 1, 2026

Teva Pharmaceuticals is recalling specific lots of Octreotide Acetate injectable suspension due to sterility concerns identified at the manufacturing facility. The FDA found quality system deficiencies that could affect the safety of the medication.

Moderate·FDA·Apr 1, 20263 products

Macleods Pharma USA is recalling Levothyroxine Sodium Tablets USP 150 mcg because they may contain less active ingredient than labeled. This means the medication may not work as intended to treat thyroid conditions. The affected lot is 16240062A with an expiration date of March 2026.

Moderate·FDA·Apr 1, 2026

Chiesi USA is recalling specific lots of CUROSURF, a medication given to premature infants to help them breathe. The company cannot confirm that all vials are sterile, which means they may be contaminated. No infections have been reported so far.

Moderate·FDA·Apr 1, 2026

Radnostix Gelatin Capsule Packs used with Sodium Iodide I-131 Kit have failed quality specifications. The affected capsules may not perform as intended. Three specific lots distributed nationwide are involved.

Moderate·FDA·Apr 1, 2026·Radnostix

Hologic's Aptima HPV Assay test kits (Master Lot 929785) may produce invalid results or false negatives, meaning they could fail to detect HPV infection. The affected kits were distributed to healthcare facilities in California, Florida, Iowa, Illinois, Missouri, North Carolina, New Mexico, Puerto Rico, and Tennessee.

Moderate·FDA·Mar 25, 2026

Diagnostica Stago's STA Liatest D-Di blood test kits are giving inaccurate measurements for D-dimer (a marker used to help rule out blood clots). The kits are showing higher-than-actual results across all test ranges. These kits are used in hospital and reference laboratories on specific analyzer machines.

Moderate·FDA·Mar 25, 2026

ConvaTec's EsteemBody Drainable Pouch (model REF:423643, 10–45mm) may leak because of a manufacturing issue. The affected pouches have lot numbers 5K00011 or 5K00714 and have been distributed worldwide. No injuries have been reported.

Moderate·FDA·Mar 25, 2026·ConvaTec3 products

Elekta has recalled certain Leksell Gamma Knife Perfexion and Icon radiosurgery systems because an adapter component may not be properly aligned or locked in place. This could affect the accuracy of radiation delivery during treatment. No injuries have been reported.

Moderate·FDA·Mar 25, 2026

Some Stryker Cub Pediatric Cribs sold in the USA are missing two warning labels on the access doors. This affects 590 cribs with specific serial numbers. No injuries have been reported.

Moderate·FDA·Mar 25, 2026

LeMaitre Vascular is recalling one unit of Artegraft Vascular Graft (Model AG740) distributed in Illinois due to a labeling mix-up on the outer packaging. The product box was labeled with an incorrect lot number, which could cause confusion during clinical use. No injuries have been reported.

Moderate·FDA·Mar 25, 2026·LeMaitre Vascular

The Welch Allyn Spot Vision Screener VS100 (software version 3.2.0.1) may display an unintended flickering screen due to a software issue. Flickering lights can trigger seizures in people who are photosensitive.

Moderate·FDA·Mar 25, 2026

The external screws that secure the cover on the Howmedica Osteonics MICS3 Angled Sagittal Saw Attachment may loosen during use and detach. This affects all units with part number 210490 distributed across the United States and several other countries. No injuries have been reported.

Moderate·FDA·Mar 25, 2026

GE is recalling three versions of Centricity Universal Viewer software, a program that displays medical images, including mammograms. User login credentials may be exposed on the local workstation, which could let an unauthorized person affect system availability or manipulate data. The recall covers 2,405 affected units, and no injuries have been reported.

Moderate·FDA·Mar 25, 20263 products

Abbott Diagnostics has recalled certain lots of the ID NOW Influenza A & B 2 test kit because they produce an unusually high number of invalid results compared to what the instructions say to expect. Invalid results mean the test does not give a clear positive or negative answer, requiring a retest.

Moderate·FDA·Mar 25, 2026

Wawa is recalling four 16 oz pint milk products sold in plastic bottles: Reduced Fat Milk 2%, Double Dutch Chocolate Milk, Cookies & Cream Milk, and Chocolate Low-fat Milk. Foreign plastic material was found on the fill line, so the milk may contain plastic pieces. The products were distributed in New Jersey, Maryland, Delaware, and Pennsylvania, and no injuries have been reported.

Moderate·FDA·Mar 25, 2026·Wawa4 products

TETAS Mireya Cherry Milkshake (Colita con Leche) popsicles contain soy lecithin that is not listed on the package label. People with soy allergies could have a serious reaction if they eat this product. About 259 units were distributed in Florida.

Moderate·FDA·Mar 25, 2026

Saputo is recalling five Clover Sonoma and Great Value products, including cottage cheese and sour cream, that may not have been fully pasteurized. The California Department of Agriculture found a broken seal on a pasteurizer, which may have affected these products. The products were shipped to stores in AL, AZ, CA, IL, MO, MS, NM, NV, UT, WA and WY, and no illnesses have been reported.

Moderate·FDA·Mar 25, 2026·Clover Sonoma5 products

BlueFrog Foods is recalling two Greenway Farms of Georgia pickle chip products sold in 16 fl oz glass jars: Garlic Dill and Jalapeno Dill. The products were packed by BlueFrog Foods and shipped to one facility in Georgia. They are being recalled because they were made without a process authority, an expert review FDA requires for certain canned foods to confirm they are processed safely.

Moderate·FDA·Mar 25, 2026·Greenway Farms of Georgia2 products

Simply Nature Spinach Bites (12 oz packages) may be contaminated with rodent hair. The affected product was distributed in Maryland and Pennsylvania. No illnesses have been reported.

Moderate·FDA·Mar 25, 2026·Simply Nature

Winder Laboratories is recalling certain batches of their grape-flavored multivitamin with fluoride chewable tablets because they contain less vitamin D than stated on the label. The FDA discovered this during an inspection. The affected products are the 0.25 mg and 1 mg formulations with specific lot numbers and expiration dates in October and November 2025.

Moderate·FDA·Mar 25, 2026·Winder Laboratories