Check a product

ReCor Medical distributed one Paradise ultrasound renal denervation catheter (Model PRDS-068-02, Lot M4907) that did not meet manufacturing standards and was supposed to be destroyed. The device was distributed in nine U.S. states. No injuries have been reported.

Moderate·FDA·Apr 8, 2026·ReCor Medical2 products

Imu-Tek Animal Health is recalling two products: Imu-Tek Colostrum-5 120-capsule bottles and Imu-Tek Colostrum-5 powder bottles. The company says the product may not have been fully processed. No injuries have been reported.

Moderate·FDA·Apr 8, 2026·Imu-Tek2 products

HEYTEA USA's Coconut Drink 1 (1L cartons) contains milk that is not listed on the label. The product was distributed to food service establishments in multiple states. This poses a serious risk to anyone with a milk allergy or severe intolerance.

Moderate·FDA·Apr 8, 2026

The Maros is recalling two prickly pear products, Mama Rose's Prickly Pear Salad Dressing (12 oz) and Prickly Pear Jelly (9 oz), both in glass bottles with gold caps. The products may contain sulfites that are not listed on the label, which can be a concern for people with sulfite sensitivity. The products were distributed in Arizona, and no injuries have been reported.

Moderate·FDA·Apr 8, 20262 products

Super World Trading is recalling three flavors of Mei Heong Yuen roasted peanuts, all 9.17 oz (260g): tangerine, walnut and garlic. The FDA says the products contain cyclamates, a sweetener banned in the United States. No illnesses have been reported. The products were distributed in 19 states, including CO, CT, DE, FL, GA, IL, MA, MD, MI, NY, NC, NJ, OH, OR, PA, TX, UT, VA and WA.

Moderate·FDA·Apr 8, 2026·Mei Heong Yuen3 products

JFE Franchising is recalling five dumpling products that may contain pieces of glass. The products are sold as Cheetos Flamin' Hot Loaded Dumpling, plus Dumpling Vegetable, Loaded Dumpling Vegetable and Dumpling Party Tray items. No injuries have been reported.

Moderate·FDA·Apr 8, 2026·JFE Franchising2 products

Divided Sunset Multi Collagen Peptides (8 oz pouch) contain egg and fish ingredients but do not clearly label them as allergens on the package. The ingredient list mentions eggshell membrane collagen and marine collagen but fails to state "EGG" or identify the fish species as required by law. This poses a risk to people with egg or fish allergies.

Moderate·FDA·Apr 8, 2026

Pocas International Corp. is recalling its Popping Boba RTD Strawberry Dragon Fruit/Oolong Tea because the packaging may not be properly sealed. This could allow the product to spoil or become contaminated. The affected product was distributed to nine states and Canada.

Moderate·FDA·Apr 8, 2026·Pocas4 products

Appco Pharma LLC is recalling prazosin hydrochloride 1mg capsules (100-count bottles) because they may contain higher-than-acceptable levels of a nitrosamine impurity. This impurity was detected during manufacturing quality checks. The recall affects specific lot numbers distributed nationwide.

Moderate·FDA·Apr 8, 2026·Appco Pharma3 products

K.C. Pharmaceuticals is recalling eight sterile eye drop products because the company cannot confirm they are sterile. The drops were sold under store and pharmacy brands including Best Choice, Walgreens, GERI CARE, LEADER, Good Sense, Industrial Eye Relief and Rugby. No injuries have been reported.

Moderate·FDA·Apr 8, 20268 products

Amneal Pharmaceuticals is recalling specific lots of tramadol 50 mg tablets because they contain higher-than-allowed levels of a chemical impurity called N-nitroso-desmethyl-tramadol (NDSRI). The impurity was discovered during stability testing of tablets nearing the end of their shelf life. No injuries have been reported.

Moderate·FDA·Apr 8, 2026

Alembic Pharmaceuticals is recalling specific lots of Bromfenac Ophthalmic Solution 0.07% because the medication failed purity and degradation tests during stability testing at 20 months. The affected eye drops may contain higher-than-acceptable impurity levels, which could affect safety and effectiveness.

Moderate·FDA·Apr 8, 2026

Nalpac is recalling DTF Sexual Chocolate because it contains sildenafil and tadalafil—prescription drug ingredients found in Viagra and Cialis—that were not listed on the label. These hidden ingredients can dangerously lower blood pressure, especially if you take nitrate medications like nitroglycerin.

Moderate·FDA·Apr 6, 2026

The USDA retracted a public health alert issued on April 1, 2026, for Walmart Great Value Fully Cooked Dino Shaped Chicken Breast Nuggets with a "Best If Used By" date of February 10, 2027. The initial alert was based on a laboratory test that showed elevated trace levels of lead, but follow-up testing found no lead contamination in the product. The USDA determined the original test result was a false positive caused by contamination in the laboratory during analysis, not in the food itself.

Moderate·USDA·Apr 6, 2026

Waldemar Link is recalling two Embrace Drill Tower instruments used in shoulder surgery, 149 units in total. The surgical technique's overview lists some article numbers incorrectly, though the individual surgical steps in the technique are correct. No injuries have been reported.

Moderate·FDA·Apr 1, 20262 products

The labeling on BD Alaris System with Guardrails Suite MX does not specify which version of Transport Layer Security (TLS) must be enabled on hospital networks for secure Wi-Fi communication with Point-of-Care Units. This could create confusion during setup and potentially leave devices with inadequate security settings.

Moderate·FDA·Apr 1, 2026

Olympus is recalling seven models of bipolar and PK/PKS cutting forceps, 3,788 units in total, used in medical procedures. The supplier did not adequately validate a welding process for components, and defective welds could cause the forceps' jaw to break during clinical use. No injuries have been reported.

Moderate·FDA·Apr 1, 20267 products

Tandem Diabetes Care insulin pumps distributed in the Czech Republic and Slovakia have translation errors in their Czech language user guide. The most serious error tells users to verify the infusion set is connected to the body when it should say the opposite—that it should NOT be connected. Following these incorrect instructions could cause unintended insulin delivery and dangerously low blood sugar.

Moderate·FDA·Apr 1, 2026

AMO has recalled certain TECNIS Eyhance intraocular lenses (IOLs) used in cataract surgery because a small number may have a defect where the lens haptic (support arm) sticks to the optic, preventing proper unfolding during implantation. This affects 361 lenses distributed across 12 U.S. states. No injuries have been reported.

Moderate·FDA·Apr 1, 2026·AMO

Straumann is recalling two custom abutment products, 20 units in total, for dental implant use. A raw material bar of TAN material was mislabeled as titanium Grade 4, so some RC Titanium abutments were made from the wrong material. The affected units were distributed in several U.S. states and in Canada. No injuries have been reported.

Moderate·FDA·Apr 1, 20262 products

Koven Technology's BiDop 3 Pocket Doppler ultrasound device was distributed with labeling that claims it can be used for fetal applications, but the FDA never approved it for that use. The device is only cleared to detect blood flow in blood vessels, not for fetal monitoring. Using it for unapproved purposes could lead to incorrect results or missed diagnoses.

Moderate·FDA·Apr 1, 2026·Koven Technology

Orthalign drill plates (Trimax-Pegged, Sizes 1–5, REF 402566) in one lot may have been made outside specifications. This could cause bone cuts larger than intended during knee surgery. Seven units were distributed in Utah.

Moderate·FDA·Apr 1, 2026·Orthalign2 products

Olympus is recalling four endoscope products because the MAJ-1443 and MAJ-1444 valves are no longer compatible with the OER-Pro and OER-Elite automated endoscope reprocessors. The recall covers about 139,000 units across the US, and no injuries have been reported.

Moderate·FDA·Apr 1, 20264 products

Beckman Coulter has recalled MicroScan Neg MIC 56 antimicrobial susceptibility testing panels (Catalog C42464, Lot 2026-01-03) due to potential contamination in the test wells. These panels are used by laboratories to identify bacteria and test antibiotic resistance. Contaminated panels could produce inaccurate test results.

Moderate·FDA·Apr 1, 2026

I.T.S. is recalling 17 orthopedic implant product lines, including bone plates and screw systems. Updated MRI safety testing found that these implants can heat up more during certain MRI conditions than the product instructions previously stated. No injuries have been reported.

Moderate·FDA·Apr 1, 2026·I.T.S17 products

GE Medical Systems' Imactis CT-Navigation System (Models E85101LA and E85101LP) has a potential issue where the needle's simulated path shown to the doctor may not match where the needle actually goes during CT-guided procedures. This discrepancy could affect the accuracy of needle placement during medical procedures. No injuries have been reported.

Moderate·FDA·Apr 1, 2026

Favorina Chocolate Ladybugs German-Style Nougat (3.52 oz) distributed by Lidl US contains tree nuts, but the label does not specify which type. This poses a risk to people with tree nut allergies who rely on ingredient labels to avoid allergens.

Moderate·FDA·Apr 1, 2026

Lucerne 2% Cottage Cheese (24 oz. tubs, UPC 0 21130 07662 8) may contain a small stainless steel spring. The spring could be present in the product and may pose a choking or injury risk if ingested or if broken pieces become sharp. No injuries have been reported.

Moderate·FDA·Apr 1, 2026·Lucerne

Mangalm is recalling six Tops GOLD pickle products from India because the mustard oil used in them may contain erucic acid. The products include mixed, mango, lime, Khatta Meetha, stuffed red chilli and green chilli pickles, in 31.74, 33.51 and 158.73 oz cans. They were distributed in California, Nevada, Oregon, Utah and Washington, and no illnesses have been reported.

Moderate·FDA·Apr 1, 2026·Tops GOLD6 products

South Florida Food is recalling Pan de Bono (frozen cheese bread) because it contains soy that is not listed on the label. This product was distributed in Florida. People with soy allergies or sensitivities could have a serious reaction if they eat it.

Moderate·FDA·Apr 1, 2026