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General Mills is recalling 2 frozen Pillsbury roll dough products, Hard Roll Dough and Kaiser Roll Dough, because they may contain small pieces of glass. About 4,340 cases were affected, distributed to stores in 19 states. No injuries have been reported.

Moderate·FDA·Jul 22, 2026·Pillsbury2 products

Nutricia is recalling two meal replacement peptide formulas in 12 oz pouches, Liquid Hope and Nourish, both in Berry Medley flavor and sold under the functional formularies name. The company found that the testing lab used the wrong method, which overstated the vitamin A content, so the products may contain less vitamin A than the label states. No injuries have been reported.

Moderate·FDA·Jul 22, 2026·Liquid Hope2 products

BD ChloraPrep Clear, a sterile skin antiseptic solution used before medical procedures, may have open or incomplete seals on individual applicator packaging. This could allow contamination of the sterile product. The issue affects multiple lot numbers distributed nationwide.

Moderate·FDA·Jul 22, 2026

Chiesi USA is recalling specific lots of CLEVIPREX (clevidipine) injectable emulsion because the manufacturer cannot guarantee the vials are sterile. This affects vials distributed nationwide with lot numbers 1239521 and 1237454, expiring in October 2027. No injuries have been reported.

Moderate·FDA·Jul 22, 2026

Bell Pharmaceuticals is recalling 11 carbamide peroxide 6.5% ear drop products, all 0.5 fl oz (15 mL), sold under store and pharmacy brands. Testing found the drops contain far less active ingredient than the label states, and their acidity is also off. No injuries have been reported.

Moderate·FDA·Jul 22, 2026·Bell Pharmaceuticals11 products

Padagis Nystatin Cream USP (100,000 units, 15 g tube, lot #205060, expiring 09/30/2027) has been recalled because stability testing found the active ingredient fell below the required strength specification. The cream may not work as effectively as intended to treat fungal infections.

Moderate·FDA·Jul 22, 2026·Padagis

PT Organics Limited is recalling select 4 oz. Pumpkin Tree Peter Rabbit Organics Banana & Strawberry fruit puree pouches sold at Kroger, Meijer, and Target between March and July 2026. An internal packaging defect may have allowed a strand of soft, food-grade plastic to enter some pouches. No injuries have been reported.

Moderate·FDA·Jul 21, 2026·PT Organics

Fresh & Ready Foods is recalling Sprig & Sprout and Fresh and Ready brand Spicy Breakfast Burritos because they may contain undeclared soy. The soy came from sausage that was inadvertently included in products labeled as vegetarian. The affected burritos were sold in grab-and-go markets and vending machines across eight southeastern states.

Moderate·FDA·Jul 21, 2026

Taylor Fresh Foods is recalling iceberg lettuce and lettuce-blend products sourced from central Mexico because they may be contaminated with Cyclospora, a parasite that causes diarrhea and other gastrointestinal symptoms. The recall affects multiple brands (CV, JB, Mark, PK, and others) distributed to 28 states from June 29 to July 16, 2026, and was prompted by a multistate outbreak.

Moderate·FDA·Jul 17, 2026·Taylor Fresh Foods

The headrest on certain Evenflo Reo by Revolve360 child seats may shift position during a crash, which could increase the risk of injury to a child. This affects specific color variants including Nantucket, Danvers, Chelsea, Holden, Brookline, and Lenox. No injuries have been reported.

Moderate·NHTSA·Jul 17, 2026

Wondermade LLC's Alabama Banana Pudding Marshmallow (4 ounce boxes) may contain small metal pieces. The issue affects 154 boxes distributed to Pennsylvania, Texas, Indiana, and Florida, with expiration dates up to July 28, 2026. No injuries have been reported.

Moderate·FDA·Jul 15, 2026·Wondermade

Wise Foods Onion Rings (3.75 oz bags) contain undeclared Yellow 5, Yellow 6, Blue 1, and unapproved Red 3 food dyes. The product was distributed in seven states. No injuries have been reported.

Moderate·FDA·Jul 15, 2026

Specialty Bakers Vanilla Dessert Shells (Giant) contain soy that is not declared on the package label. People with a soy allergy or sensitivity who eat these shells without knowing they contain soy could have an allergic reaction. The affected product was distributed in Pennsylvania.

Moderate·FDA·Jul 15, 2026

Bakr Brown Butter Chocolate Chunk Ready to Bake Cookie Dough contains soy that is not declared on the package label. This product was sold at Target stores in Southern California, Southern Nevada, Arizona, and Utah starting in June 2026. People with a soy allergy or sensitivity could have a serious reaction if they eat this product.

Moderate·FDA·Jul 15, 2026

Adams Extract & Spice LLC is recalling Johnny's Salad and Pasta Elegance seasoning in 2.75 oz and 5.5 oz sizes because the product contains sesame but does not declare it on the label. People with a sesame allergy who consume this product could have an allergic reaction.

Moderate·FDA·Jul 15, 20265 products

Certain sterile tourniquet extension hoses may have a breach in the sealing area of the sterile pouch, which could allow contamination. If used without detection, the hose could potentially cause a moderate localized infection at the surgical site.

Moderate·FDA·Jul 8, 20262 products

W L Gore & Associates has recalled specific batches of the GORE TAG Thoracic Branch Endoprosthesis Side Branch Component due to a risk of catheter separation during use. This is a surgical implant used to repair certain aortic conditions. The separation could potentially affect the device's ability to function as intended.

Moderate·FDA·Jul 8, 2026·Gore

Masimo is recalling two Radius VSM products: an ECG pre-connected electrode set and disposable blood pressure cuffs, covering 1,800 units in total. The ECG feature may incorrectly flag abnormally slow or fast heart rates in patients with normal rhythms, which could distract clinicians from true alarms and delay treatment. The blood pressure cuffs may have rough edges that can cause skin irritation or redness. No injuries have been reported.

Moderate·FDA·Jul 8, 2026·Masimo Corporation2 products

Laborie Medical Technologies' Solar GI System water perfusion devices may accumulate moisture inside tubing, filters, and pressure sensors during extended clinical use. This moisture buildup can affect how the system measures airflow and pressure, potentially impacting test results.

Moderate·FDA·Jul 8, 2026·Laborie Medical Technologies Corp

Bard Access Systems is recalling 14 products, including PICC, midline, and dialysis catheters and biopsy trays. The recall stems from lidocaine ampoules that were made under deficient manufacturing practices, and the supplier is recalling them. No injuries have been reported.

Moderate·FDA·Jul 8, 202614 products

BD Switzerland inadvertently shipped 50 engineering sample units of the Medline 111 Gravity Set with 3 Needle Free Y-Sites into the U.S. market. These units were labeled "Not for Human Use" and were not intended for patient care. No injuries have been reported.

Moderate·FDA·Jul 8, 2026

The Shiley Disposable Decannulation Plug (DDCP), a red connector used on tracheostomy tubes to block airflow, carries labeling that incorrectly indicates it does not contain DEHP (a chemical compound). The product actually contains 30–35% DEHP. Users relying on the label may not be aware of DEHP exposure during use.

Moderate·FDA·Jul 8, 2026

Certain Zeiss Intrabeam Spherical Applicator 1.5 cm units used in intraoperative radiation therapy did not meet manufacturing specifications. A total of 13 units were affected across the United States, Puerto Rico, and several other countries. No injuries have been reported.

Moderate·FDA·Jul 8, 2026·Carl Zeiss Meditec

Siemens has identified a potential issue with the Display ceiling suspension (DCS Fix XL) component on ARTIS icono ceiling systems. Over time, screws that secure the monitor to the suspension may gradually loosen, which could affect the stability of the mounted display.

Moderate·FDA·Jul 8, 2026

RayCare 2024A SP1 oncology information system has a software issue where beam set delivery notes can lose data if modified at the same time or updated during an active treatment session. Users may not be notified when these changes occur, potentially affecting treatment records.

Moderate·FDA·Jul 8, 2026·Raysearch Laboratories2 products

Some Medela ENFit ExSet enteral extension sets contain incorrect connectors that may not attach properly to ENFit connections. This incompatibility could cause a slight delay in delivering nutrition or medication through the feeding tube.

Moderate·FDA·Jul 8, 2026·Medela Inc

In some cases, the collimator (a precision component) may not fully dock into the Cyberknife treatment system. This triggers a safety interlock that blocks motion from the operator console. However, if staff enter the treatment room and use the in-room control pendant to move the system, the collimator can release and fall from its housing, creating a potential impact hazard.

Moderate·FDA·Jul 8, 2026·Accuray Incorporated

Siemens is recalling three models of its ARTIS icono imaging systems, 234 units in total, because the detector lift may stop moving after it is adjusted to its highest or lowest height limit. No injuries have been reported.

Moderate·FDA·Jul 8, 20263 products

In some cases, the collimator (a precision component) may not fully dock into the Cyberknife system. If operators bypass the safety interlock by using the in-room control pendant, the collimator can release and fall from the machine housing. This affects 48 Cyberknife units worldwide running software version 11X or earlier.

Moderate·FDA·Jul 8, 2026·Accuray Incorporated

Pilling Wecksorb Neurosponges—sterile cotton sponges used during brain and spine surgery—may contain higher-than-safe levels of endotoxins (bacterial toxins). The affected sponges were manufactured between 2021 and 2024. No injuries have been reported, but elevated endotoxins could trigger an inflammatory response during surgery.

Moderate·FDA·Jul 8, 2026·TELEFLEX LLC