https://www.fda.gov/consumers/consumer-updates/fda-101-product-recalls
Recalls are typically voluntary actions taken by a company to remove or correct products on the market that violate U.S. Food and Drug Administration laws and...
product recallsfda
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/blue-ridge-beef-recalls-product-because-possible-health-risk?source=govdelivery&utm_medium=email&utm_source=govdelivery
Blue Ridge Beef is voluntarily recalling one (1) of its frozen products due to their potential to be contaminated with Listeria monocytogenes. Listeria can...
blue ridgepossible healthbeefrecallsproduct
https://www.foxbusiness.com/lifestyle/fda-recalls-blood-pressure-medication-cholesterol-drug-contamination
The FDA issued a Class III recall of 11,100 bottles of Ziac blood pressure medication after discovering cross-contamination with ezetimibe cholesterol drug.
blood pressure medicationfda recallsduecontaminationconcerns
https://www.tpr.org/2018-12-04/too-much-vitamin-d-in-dog-food-may-have-poisoned-pets-spurring-recalls-and-fda-alert
The FDA says pet owners should watch out for vitamin D toxicity. Recalled brands include Abound, Nutrisca and Natural Life.
dog foodmuchvitaminmaypoisoned
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/siluetaya-recalls-tejocote-product-because-possible-health-risk
SiluetaYa is recalling its tejocote root because FDA analysis has determined that the products appear to be Thevetia peruviana, or yellow oleander. All parts...
possible healthrecallstejocoteproductrisk
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/mountain-rose-herbs-recalls-organic-kudzu-root-herbal-supplement-due-possible-health-risk
Mountain Rose Herbs (MRH) of Eugene, Oregon is recalling all sizes of its Organic Kudzu Root Herbal Supplement from Lot #24247-X and #24247 because they have...
mountain rose herbskudzu rootherbal supplementrecallsorganic
https://www.fda.gov/safety/archive-recalls-market-withdrawals-safety-alerts/2018-recalls-market-withdrawals-safety-alerts
2018 Recalls, Market Withdrawals & Safety Alerts
safety alertsrecallsmarketwithdrawalsfda
https://www.hmpgloballearningnetwork.com/site/pln/content/fda-recalls-anti-epileptic-drug
A Class III, nationwide recall of Clonazepam Tablets, USP, 0.5 mg, was announced in the latest US Food and Drug Administration (FDA) Enforcement Report. Drug...
fda recallsanti epilepticdrug
https://www.fda.gov/medical-devices/medical-device-recalls-and-early-alerts/insulet-corporation-recalls-omnipod-5-android-app-due-software-error
Omnipod 5 App recalled due to a software error which occurs when users input bolus amounts below 1 unit without adding a zero before the decimal point.
android appinsuletcorporationrecallsomnipod
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/wakefern-food-corp-voluntarily-recalls-shoprite-semi-sweet-real-chocolate-chips
Wakefern Food Corp. has initiated a voluntary recall of its ShopRite brand Semi-Sweet Real Chocolate Chips. The chips were sold in 24 oz. bags bearing a UPC...
wakefern foodsemi sweetreal chocolatecorpvoluntarily
https://www.fda.gov/medical-devices/medical-device-recalls-and-early-alerts/draeger-recalls-carina-sub-acute-care-ventilators-contaminants-airpath
Contaminants exceed acceptable levels if used by pediatric patients for more than 30 days.
acute caredraegerrecallscarinasub
https://www.scrippsnews.com/life/recalls/fda-recalls-popular-diabetes-care-app-after-glitches-result-in-injuries-to-224-patients
A glitch in a version of Tandem Diabetes Care's Apple iOS app that is used with certain insulin pumps has led to over 200 injuries, prompting the FDA to issue...
fda recallsdiabetes careappglitchesresulted
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/sno-pac-foods-recalls-del-mar-35-lb-bulk-frozen-spinach-and-10-oz-organic-frozen-cut-spinach
Sno Pac Foods of Caledonia, MN, is recalling Del Mar 35 LB Bulk Organic Frozen Spinach and Sno Pac10 oz Organic Frozen Cut Spinach because they have the...
del marsnopacfoodsrecalls
https://www.prevention.com/health/a69496819/jenis-ice-cream-recall-passionfruit-dreamsicle/
Nov 21, 2025 - A batch of Jeni’s Splendid Ice Cream Passion Fruit Dreamsicle Ice Cream Bars is being recalled over undeclared allergens, per the FDA.
ice creamrecallspopularflavornationwide
https://www.fda.gov/vaccines-blood-biologics/safety-availability-biologics/recalls-biologics
Biologic recalls are listed by year. Recalls are a firm's removal or correction of a marketed product that the FDA considers to be in violation of the laws it...
recallsbiologicsfda
https://www.natureworldnews.com/articles/59716/20231130/fda-expands-cantaloupe-recalls-salmonella-infections-affects-32-states.htm
As a result of the contaminated cantaloupe, nearly 100 people in 32 states have become sick. Read more here.
salmonella infectionsfdaexpandscantalouperecalls
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/cooperstown-cheese-company-recalls-products-because-possible-health-risk
Cooperstown Cheese Company of Milford, NY, is recalling 1400 pounds of cheese purchased, sold or distributed from June 21, 2023 to July 10, 2023 because it has...
cheese companypossible healthcooperstownrecallsproducts
https://www.cbsnews.com/news/fda-medical-device-recalls-stay-in-use/
With medical devices, recalls are not always what they seem. In some recalls, including some of the most serious, the FDA and the manufacturers let doctors and...
medical devicesfdacallsyettargeted
https://bestlifeonline.com/oysters-clams-norovirus-december-2024/
In two separate recall notices, the FDA has warned that oysters and Manila clams may be contaminated with norovirus.
fda recallsoystersclamslinkednorovirus
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/eagle-produce-llc-recalls-whole-cantaloupe-because-possible-health-risk-0
Eagle Produce LLC Scottsdale, AZ is initiating a recall of 224 cases of whole cantaloupe because they have the potential to be contaminated with Salmonella....
possible healtheagleproducellcrecalls
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/pro-sports-club-recalls-yogurt-peanut-crunch-bar-because-possible-health-risk
Pro Sports Club of Bellevue, WA is recalling 36.957 Yogurt Peanut Crunch bars because it may be contaminated with Escherichia coli H7 bacteria (E.Coli O157:H7)...
pro sportscrunch barclubrecallsyogurt
https://www.foxla.com/news/fda-warns-there-could-be-more-salmonella-related-recalls
There has been a string of voluntary recalls due to salmonella fears recently, and while federal officials have identified the possible source, they say it...
fdawarnscouldsalmonellarelated
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts?search_api_fulltext=ranitidine&field_regulated_product_field=All
FDA and industry press releases regarding product recalls
safety alertsrecallsmarketwithdrawalsfda
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/hh-fresh-trading-corp-recalls-taiwan-enoki-200gx25pk-because-possible-health-risk
Because they have the potential to be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young...
hhfreshtradingcorprecalls
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/panera-bread-preemptively-recalls-all-2-oz-and-8-oz-cream-cheese-products
While there have been no reported illnesses, out of an abundance of caution, Panera Bread is conducting a nationwide preemptive, voluntary recall of all 2 oz....
panera breadrecallsoz
https://www.fda.gov/drugs/drug-safety-and-availability/drug-recalls?msclkid=9f0e8a16aaf011ec8bf54688b489ed9e
FDA provides a searchable list of recalled products. Drug recalls are actions taken by a firm to remove a product from the market and may be conducted on a...
drug recallsfda
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/fudgeamentals-recalls-fudge-made-jif-peanut-butter-because-possible-health-risk?permalink=3F32CF26B84DFC9A1D4616B9A466AD96617B8B7E32F4AB3C2D915CB3F85C5799
Fudgeamentals of Melville, New York is voluntarily recalling fudge under the Fudgeamentals and Walmart brands made with Jif Peanut Butter, packaged in 8 oz....
jif peanut butterrecallsfudgemade
https://www.fda.gov/medical-devices/medical-device-recalls-and-early-alerts/philips-recalls-brightview-imaging-systems-due-detector-unexpectedly-falling
If the detector support component fails, imaging cannot be completed, and the detector may contact the patient.
imaging systemsphilipsrecallsbrightviewdue
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/ziegenfelder-company-recalls-certain-ice-pops-possible-health-risk
As a precaution, the Ziegenfelder Company of Wheeling, WV is voluntarily recalling approximately 3,000 cases of Budget $aver Cherry Pineapple Monster Pops and...
ice popspossible healthcompanyrecallscertain
https://www.fda.gov/inspections-compliance-enforcement-and-criminal-investigations/enforcement-story/recalls-fiscal-year-2002-fda-center
Recalls for Fiscal Year 2002 by FDA Center
fiscal yearrecallsfdacenter
https://www.drugwatch.com/news/2012/07/10/johnson-johnson-mesh-recalls-fda/
Johnson and Johnson proposed a recall of four transvaginal mesh products to the FDA that allows it to avoid expensive safety studies.
johnsondictatesrecallsfda
https://www.fda.gov/drugs/drug-safety-and-availability/limited-number-voluntary-recalls-initiated-after-fda-testing-acne-products-benzene-findings-show?utm_medium=email&utm_source=govdelivery
Voluntary recalls of acne products after FDA testing finds small number of proudcts with elevated levels of benzene
voluntary recallslimitednumberinitiatedfda
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/lords-organics-recalls-ginger-powder-because-possible-health-risk
LORDS ORGANICS is recalling Ginger Powder Product from AGF Organic Veda, because it has the potential to be contaminated with Salmonella, an organism which can...
ginger powderpossible healthlordsorganicsrecalls
https://www.pressenza.com/2025/11/ecowaste-coalition-urges-fda-to-test-play-sand-products-for-asbestos-following-recalls-in-australia-and-new-zealand/
Nov 18, 2025 - 18 November 2025, Quezon City, Philippines. The toxics watchdog group EcoWaste Coalition urged the Food and Drug Administration (FDA) to analyze colored
ecowaste coalitiontest playsand productsurgesfda
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/aquastar-usa-corp-recalls-cocktail-shrimp-6oz-because-possible-health-risk
August 28, 2025, AquaStar (USA) Corp of Seattle, WA is recalling approximately 26,460 packages of Cocktail Shrimp 6oz (see photo), imported from Indonesia,...
cocktail shrimpaquastarusacorprecalls
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/snapchill-llc-recalls-canned-coffee-products-due-potential-clostridium-botulinum
Snapchill LLC (Snapchill) of Green Bay, WI is voluntarily recalling all canned coffee products manufactured by the company, within expiration date, because...
canned coffeellcrecallsproductsdue
https://www.raps.org/news-and-articles/news-articles/2025/7/investment-in-quality-management-can-reduce-defect
Companies that invest in quality management initiatives can incur lower costs related to defects, waste, and recalls compared to those that do not make such...
quality managementinvestmentreducedefectsrecalls
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/becca-cosmetics-voluntarily-recalls-light-shifter-brightening-concealer
Out of abundance of caution, and in line with its commitment to consumer satisfaction and safety, Becca Cosmetics is voluntarily recalling all shades of its...
becca cosmeticsvoluntarilyrecallslightshifter
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/new-age-international-recalls-signature-enoki-mushrooms-due-potential-health-risk
New Age International Inc of Brooklyn, NY 11206 is recalling its 200g (7.05OZ) packaged of Signature Enoki Mushroom, Product of K Food (Korea Food Signature)...
new ageenoki mushroomsinternationalrecallssignature
https://www.fda.gov/medical-devices/medical-device-recalls-and-early-alerts/eitan-medical-ltd-recalls-sapphire-infusion-pumps-failure-detect-air-line
Sapphire Infusion Pumps are being recalled because they may fail to detect air in the line. The failure could cause injury or death.
infusion pumpseitanmedicalltdrecalls