Search by meaning, not just keywords: describe the product or the hazard and we find matching recalls even when the official notice uses different words. Brand names and model numbers work too.
Latest recalls
35,004 found- Use cautionMedical device
ROi CPS LLC recalls Custom procedure packs, containing Clearlink Continu-Flo, labeled as follows: a) regard LD00200L-VAG DELIVERY MOTHER -
ROi CPS LLC recalls custom procedure packs with Clearlink Continu-Flo devices due to potential incorrect use during surgical procedures. Affected items include specific model numbers and lot numbers.
ROi CPSJan 3, 2020 - Lower riskFood
Jeni's Splendid Ice Creams LLC recalls Jeni's Dairy Free Cold Brew with Coconut Cream Pints frozen dessert
Jeni's Dairy Free Cold Brew with Coconut Cream Pints may contain undeclared milk allergen. Consumers should check lot numbers 19-016, 19-086, 19-154, 19-241 for affected products.
Jeni'sJan 3, 2020 - Lower riskFood
Ducktrap River of Maine LLC recalls Ducktrap River of Maine Herring Center Cuts in Wine Sauce, 12 oz.
Ducktrap River of Maine recalls 12 oz. Herring Center Cuts in Wine Sauce (sold by Jul 29, 2020) due to undeclared milk. Consumers should check UPC 082674072408 for affected products.
Ducktrap River of MaineJan 3, 2020 - Stop using nowMeat & poultry
FSIS Issues Public Health Alert for Products Associated with the FDA Almark Foods Recall Due to Possible Listeria Monocytogenes Contamination
FSIS recalls Almark Foods hard boiled egg products due to possible Listeria monocytogenes contamination. Consumers should not consume these products and dispose of them immediately.
Almark FoodsJan 2, 2020 - Lower riskMedical device
ICU Medical, Inc. recalls Central Venous Catheters are indicated for the assessment of hemodynamic status through right atrial, right
ICU Medical recalls certain central venous catheters due to guidewire not passing through needles, which may affect hemodynamic monitoring. Affected units have specific model and lot numbers.
ICU MedicalJan 2, 2020 - Use cautionMedical device
Clinical Diagnostic Solutions, Inc. recalls Medonic M-Series Hematology Analyzer M16S BD ABR US Product code: 1400075; OUS Product code 1400011
Clinical Diagnostic Solutions recalls Medonic M16S hematology analyzers with serial numbers before 3/21/2019 due to possible misidentification of sample results and operator needle injury risk.
Clinical Diagnostic SolutionsJan 2, 2020 - Stop using nowFood
purely elizabeth. recalls purely elizabeth Chocolate Sea Salt probiotic granola. Net Wt. 8 oz (227g). UPC 55140-00268. Made with organic quinoa,
Purely Elizabeth recalls Chocolate Sea Salt probiotic granola due to undeclared walnut allergen. Check your UPC and lot number for details.
Purely ElizabethJan 2, 2020 - Use cautionMedical device
ulrich medical USA Inc recalls Ulrich medical neon3 OCT spinal stabilization, REF CS 3917-12, Locking screw for crosslink, screw-to-screw
Ulrich Medical recalls neon3 OCT spinal stabilization screws with lot numbers U010577, U016620, U019084 due to potential torque failure during installation. Affected units may not hold properly under required force.
Ulrich MedicalDec 31, 2019 - Lower riskMedical device
Koios Medical, Inc. recalls Koios DS Breast <series 1.0>. The device is a software application which assists skilled physicians in analyzing breast
Koios Medical recalls software versions 1.2 to 1.6 for breast ultrasound analysis due to insufficient quality documentation. Affected versions may not meet regulatory standards.
KoiosDec 31, 2019 - Use cautionFood
Dianne's Fine Desserts recalls Sienna Chocolate Turtle Brownie (frozen); 108 OZ (6.75 LB) Uncut, 4 trays per case; UPC: 93901541857 SSC:10093901541854
Dianne's Fine Desserts recalls 108 oz frozen brownies due to undeclared peanuts. Consumers should avoid these products to prevent allergic reactions.
Dianne's Fine DessertsDec 31, 2019 - Lower riskFood
SANITY CHOCOLATE recalls Dark with Browned Ghee is wrapped in a foil and jacketed with black paper. There is a white sticker on the front that
Sanity Chocolate recalls Dark with Browned Ghee bars due to missing milk declaration on labels. Consumers should check for the white sticker and batch name on the back label.
Sanity ChocolateDec 31, 2019 - Lower riskFood
Rachael's Food Corporation recalls Rachael's brand and Big Y brand Protein Snack Packs; containing one hard boiled egg, diced roasted turkey, and roasted
Rachael's Food Corporation recalls Protein Snack Packs with Listeria monocytogenes risk. Products contain hard-boiled egg, turkey, almonds. Check codes: Rachael's 81190701592 or Big Y 01889490543.
Rachael'sDec 31, 2019 - Lower riskMeat & poultry
J&J Distributing Recalls Salad Products Due to Misbranding and Undeclared Allergens
USDA FSIS recalls 136 pounds of ready-to-eat salads with undeclared pine nuts (tree nut) due to misbranding. Consumers urged not to consume and dispose of products.
J&J DistributingDec 30, 2019 - Use cautionMedical device
Solta Medical Inc recalls Thermage Face Tip 3.0, REF/UDI: TTNS3,00C3-400/UDI (01)000850608002377; REF TTNS3.00C3-600/UDI (01)000850608002384; REF
Solta Medical recalls Thermage Face Tip 3.0 devices with specific model numbers due to complaints of sparking during RF surgical procedures, which may cause skin burns. Affected units include certain production dates and lot numbers.
Solta MedicalDec 30, 2019 - Lower riskMedical device
Smith & Nephew, Inc. recalls TwinFix Ti 2.8 mm HS Suture Anchor - Product Usage: A fixation device intended to provide secure attachment of soft
Smith & Nephew recalls TwinFix Ti 2.8 mm HS Suture Anchor due to potential sterile barrier breach from protective tube dislodging, risking device contamination.
Smith & NephewDec 30, 2019 - Lower riskMedical device
Philips North America, LLC recalls Integris Allura 9, system codes 722018 722021
Philips recalls specific Integris Allura 9 X-ray systems (model codes 722018-722021) due to capacitor failure after surges, preventing image acquisition. Affected units may need repair.
PhilipsDec 30, 2019 - Use cautionFood
Meijer recalls Fresh From Meijer diced hard boiled eggs sold by weight from the salad bar area in clear plastic clamshell PLU 8505,
Meijer recalls diced hard boiled eggs sold by weight from salad bars with PLU 8505 due to possible Listeria contamination. All products with best by dates affected, last sold December 30, 2019.
MeijerDec 30, 2019 - Use cautionFood
Savannah Food Company, Inc. recalls Savannah Classics Classic Bread Stuffing packaged in 4.5lb trays
Savannah Food Company recalls Classic Bread Stuffing (4.5lb trays) due to possible listeria contamination. Consumers should avoid products with lot numbers 1014191: 38025 from 10/2021.
Savannah FoodDec 30, 2019 - UnratedFood
International Sprout Holding Inc. recalls Clover seed in 50 lb. woven poly bags, 40 bags to a pallet.
International Sprout Holding Inc. recalls Clover seed in 50 lb. woven poly bags (40 bags per pallet) due to possible E. Col: contamination. Consumers should check product details.
CloverDec 30, 2019 - Lower riskMedical device
Wright Medical Technology, Inc. recalls WRIGHT EVOLVE Proline Head, Size: +2, OD: 20mm, REF 496H220
Wright Medical recalls EVOLVE Proline Head Size +2, OD 20mm (REF 496H220) due to incorrect labeling and laser marking. Affected units may have wrong size product.
Wright MedicalDec 27, 2019 - Lower riskMedical device
Cook Inc. recalls Dawson-Mueller Drainage Catheter, Multipurpose Drainage Catheter, RPN UL T6.3-35-15-P-5S-CLDM-HC, UL T6.
Cook recalls specific lots of Dawson-Mueller Drainage Catheter due to potential leakage from Mac-Loc hub assembly. Affected units may cause fluid buildup; contact for return or replacement.
CookDec 27, 2019 - Stop using nowDrug
RemedyRepack Inc. recalls Ketorolac Trom, 30 mg/1mL Inj. for I.V./I.M. Use, Rx Only, QTY: 1 ml, Repackaged by: RemedyRepack Inc., Indiana, PA
RemedyRePack recalls Ketorolac Trom injections due to small black particles found during visual inspection. Affected products have specific NDC and lot numbers. Stop using immediately.
RemedyRePackDec 27, 2019 - Use cautionFood
Cheesewich Factory recalls RTE bacon and eggs 3.6 oz package
Cheesewich Factory recalls 3.6 oz RTE bacon and eggs packages with potential Listeria Monocytogenes contamination. Consumers should check product dates and lot codes for affected items.
Cheesewich FactoryDec 27, 2019 - Stop using nowFood
Fresh Unlimited Inc recalls Chef Salad Kit: 8lbs packaged in cardboard box
Fresh Unlimited Inc recalls 8lb Chef Salad Kits due to potential Listeria monocytogenes contamination. Check your product dates and locations immediately.
Fresh Unlimited IncDec 27, 2019 - Use cautionFood
Sun Valley Foods recalls 3.1-oz. packages containing "EGGLANDS BEST HARD-COOKED EGG BACON & CHEDDAR"
Sun Valley Foods recalls 3.1-oz. hard-boiled egg bacon & cheddar products with potential Listeria monocytogenes contamination. Consumers should check expiration dates and take action if affected.
Sun Valley FoodsDec 27, 2019 - Use cautionFood
Five Star Gourmet Foods of Florida recalls Simply Fresh brand MiniMeals2Go Avocado Toast (6.75 OZ) ready-to-eat snack packs
Five Star Gourmet Foods of Florida recalls Simply Fresh MiniMeals2Go Avocado Toast snack packs due to potential Listeria monocytogenes contamination. Affected lots include 34619, 34719, 35019, 35119, 35219, 35719.
Simply FreshDec 27, 2019 - Lower riskMedical device
Cardinal Health Inc. recalls Kangaroo Connect ENPlus Spike Set Anti-free Flow, Product Code 77000FD
Cardinal Health recalls Kangaroo Connect ENPlus Spike Set Anti-free Flow (Product Code 77000FD) due to potential leaks at the tube and spike connector interface. All units are affected.
Cardinal HealthDec 26, 2019 - Lower riskDrug
Lupin Pharmaceuticals Inc. recalls Blisovi Fe 1.5/30 (norethindrone acetate and ethinyl estradiol tablets USP and ferrous fumarate tablets 75mg), Rx Only,
Lupin Pharmaceuticals recalls Blisovi Fe 1.5/30 tablets due to complaints of crumbling tablets when removed from blister packs. This may affect prescription users.
Lupin PharmaceuticalsDec 26, 2019 - Stop using nowDrug
AAA Pharmaceutical, Inc. recalls Ranitidine 150 mg tablets, 24 count bottles, NDC 37808-196-01.
AAA Pharmaceutical recalls 150 mg Ranitidine tablets (24 count) with NDMA impurity found in manufacturing. Consumers should stop using these products immediately.
AAA PharmaceuticalDec 26, 2019 - Lower riskDrug
Akorn, Inc. recalls Proparacaine Hydrochloride Ophthalmic Solution, USP, 0.5%, 15 mL per dropper bottle, Sterile, Rx Only, Manufactured by:
Akorn recalls 0.5% Proparacaine Hydrochloride Ophthalmic Solution due to chemical contamination in equipment cleaning residue. This may cause unsafe results for eye procedures.
AkornDec 26, 2019
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