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
34,891 found- Use cautionMedical device
Intuitive Surgical, Inc. recalls da Vinci Xi Surgical System Product Usage: The da Vinci Xi Surgical System (IS4000) is designed to assist a surgeon in
Intuitive Surgical recalls da Vinci Xi Surgical System (IS4000) units with potentially under-torqued brake screws in patient side carts. This could cause system arm movement during surgery, risking patient injury. Affected units have specific serial numbers listed in the recall.
Intuitive SurgicalJun 1, 2017 - Lower riskMedical device
Master & Frank (Pinghu) Co., Ltd. recalls MEDLINE SIRUS Surgical Gown, Strong Protection, Poly-Reinforced, Breathable Film Sleeve, XXL-XLONG Sterile Single-Use
MEDLINE recalls sterile surgical gowns with potential fluid leakage through sleeve seams. Learn product details and safety steps to avoid infection risks during medical procedures.
MEDLINEJun 1, 2017 - Lower riskMedical device
Dukal Corp. recalls BLUE BURN SHEET, STERILE, 60" x 96"; Item 7305, GAM item 30-01 Product Usage - May provide a sterile, barrier
Dukal Corp. recalls sterile burn sheets (Item 7305) with shredded sheets in carton. Affected lots include JT13607 to JT36212. Consumers should check lot numbers and contact for details.
Dukal Corp.Jun 1, 2017 - Lower riskMedical device
Arrow International Inc recalls ARROW¿ PICC powered by ARROW¿ VPS¿ Stylet The Pressure Injectable PICC is indicated for short or long term peripheral
Arrow International recalls PICC kits that might have 5Fr instead of 4Fr peel-away sheaths. This could cause complications during medical procedures. Affected kits have specific lot numbers.
ArrowJun 1, 2017 - Lower riskMedical device
Shippert Medical Technologies recalls Tissu-Trans Filtron 500, 3-TT-FILTRON 500. Product Usage: Intended for fat transfer and liposuction.
Shippert Medical Technologies recalls Tissu-Trans Filtron 500 devices due to potential seal failure in sterile packaging. Affected units include specific lot numbers for fat transfer and liposuction procedures.
Shippert Medical TechnologiesJun 1, 2017 - UnratedDrug
MedPark Pharmacy, LLC recalls methylcobalamin 1mg/1mL, vial for injection, Rx only, MedPark Pharmacy 2002 Medical Pkwy. # 170 Annapolis, MD 21401
MedPark Pharmacy recalls methylcobalamin 1mg/1mL vials for injection due to lack of sterility assurance. This product was sold with specific lot numbers and expiration dates.
MedPark PharmacyJun 1, 2017 - Lower riskDrug
American Pharmaceutical Ingredients LLC recalls Doxycycline Hyclate USP, active pharmaceutical ingredient, a) 25 g packaged in a 500 cc container (NDC: 58597-8082-4),
American Pharmaceutical Ingredients LLC recalls Doxycycline Hyclate USP (NDCs 58597-8082-4 to 58597-8082-8) for misbranding on FDA Import Alert 66-66. Affected items are prescription compounding ingredients.
American Pharmaceutical IngredientsJun 1, 2017 - UnratedDrug
Xttrium Laboratories Inc recalls Chlorhexidine Gluconate 0.12% Oral Rinse, USP, 1 Pint (473 ml), Rx Only, Distributed by: Xttrium Laboratories, Inc.,
Xttrium Laboratories recalls 0.12% Chlorhexidine Gluconate oral rinse due to CGMP deviations. Affected lots 704-201 (exp 03/20) and 705-208 (exp 04/20) were distributed in 1999. No remedy specified in recall notice.
Xttrium LaboratoriesJun 1, 2017 - Lower riskDrug
Lucid Pharma LLC recalls Venlafaxine Hydrochloride Extended-Release Capsules USP, 75 mg, packaged in a) 30-count bottles (NDC 52343-132-30) and
Lucid Pharma recalls 75mg Venlafaxine Extended-Release Capsules due to reports of melted capsules in some bottles. This may affect safety and requires checking your product.
Lucid PharmaJun 1, 2017 - Lower riskDrug
L. Perrigo Company recalls Option 2, Levonorgestrel Tablet, 1.5 mg, Emergency Contraceptive, 1 Tablet per box, Distributed By Perrigo, Allegan, MI
L. Perrigo recalls Option 2 emergency contraceptive tablets (1.5 mg) due to missing tablet blister strips in some boxes. Affected lots expire by April 2018 or July 2018.
L. Perrigo CompanyJun 1, 2017 - Lower riskFood
AB HANSON AND MOHRING recalls Salinity sea salt Saltwell, Saltwell 57 and Saltwell for Organic Use 50 lb. bags
AB Hanson and Mooring recalls Salinity sea salt bags (Saltwell, Saltwell 57, Organic Use) due to foreign material. Affected lots include AS08040117 through AS08270117. Consumers should check their bags for foreign material and contact the company.
AB Hanson and MooringJun 1, 2017 - Lower riskFood
Schnucks Markets Corporate Office recalls Schnucks Bakery, Sliced Pudding Cake Tray, NET WT 2.00 lb (907 g)
Schnucks recalls sliced pudding cake trays that may contain walnuts but lack walnut labeling on the scale. This could cause allergic reactions for those with nut allergies.
SchnucksJun 1, 2017 - Use cautionConsumer product
Kreative Kids Recalls Children's Robes Due to Violation of Federal Flammability Standard
Kreative Kids recalls eight styles of children's polyester robes sold in sizes 4-6 and : risk of burns due to flammability standards violation. Consumers should stop using and get a refund.
Kreative KidsJun 1, 2017 - Use cautionVehicle
SPARTAN GLADIATOR (2014) recall — Electrical System
Spartan is recalling 2014 Gladiator vehicles with a starter motor that may overheat and cause fire. Owners must contact Spartan for free replacement.
SpartanMay 31, 2017 - Use cautionVehicle
PIERCE ARROW XT (2016) recall — Suspension
Pierce is recalling certain 2012-2017 Arrow XT fire trucks with T3 rear steer option due to potential sway bar detachment causing vehicle swaying during steering, increasing crash risk.
PierceMay 31, 2017 - Lower riskVehicle
VOLKSWAGEN JETTA (2017) recall — Equipment
Volkswagen recalls 2017 Jetta vehicles with mismatched VINs that fail regulatory compliance. Owners must contact customer service for free replacement.
VolkswagenMay 31, 2017 - UnratedMedical device
Soft Computer Consultants, Inc. recalls SoftLab Software Laboratory information system to be used in a medical research or clinical laboratory by
SoftLab Software versions 4.5.4.3-4.5.5.20 recalled for incorrect lab result display due to LOINC code errors. Affected medical labs must stop using these versions immediately.
Soft Computer ConsultantsMay 31, 2017 - Lower riskMedical device
Becton Dickinson & Company recalls BD Precision Glide Needle 18G x 1 RB, Catalog 305195 Product Usage: These needles are intended for general purpose
Becton Dickinson recalls BD Precision Glide Needle 18G x 1 RB (Catalog 305195) due to hub damage causing breakage or leakage during use. Affected units sold with lot number 6152995 through expiration date 31-Jul-21.
Becton DickinsonMay 31, 2017 - Use cautionMedical device
Philips Electronics North America Corporation recalls Philips DuraDiagnost X-ray systems: DuraDiagnost (R1.0, Product Number 712210) DuraDiagnost (R2.0, Product Number
Philips recalls DuraDiagnost X-ray systems with cracked welding joints that could cause tube arm assembly to fall. Affected models include R1.0 (712210), R2.0 (712211), and R3.0 (712211) with specific serial numbers.
PhilipsMay 31, 2017 - Lower riskMedical device
Encore Medical, Lp recalls 3DKNEE(TM) SYSTEM e+, tibial Insert, LEFT Sz 6 / 11mm, REF 391-11-706, QTY 01, The 3DKnee Insert HXL Tibial Inserts are
Encore Medical recalls 3DKNEE System e+ Left Size 6 Tibial Insert (REF 391-11-706) due to mispacking: a Size 6 box contains a Size 8 insert. This affects patients using knee implants.
Encore MedicalMay 31, 2017 - Lower riskDrug
Teva Pharmaceuticals recalls Paliperidone Extended-Release Tablets, 3 mg, 90 count bottles, Rx only, Manufactured by: Actavis Laboratories FL, Inc.,
Teva recalls 3mg Paliperidone Extended-Release Tablets due to potential drug release issues found in stability testing. Affected lots may have tablets that don't dissolve properly.
Teva PharmaceuticalsMay 31, 2017 - Lower riskFood
Blue Diamond Growers recalls Blue Diamond Almonds Blanc DCD FN C (blanched diced fine); NET WT 11.34 Kg, 25 lbs. corrugated carton with poly liner;
Blue Diamond Growers recalls blanched diced fine almonds due to Salmonella contamination found in customer testing. Consumers should check product details and follow safety steps.
Blue DiamondMay 31, 2017 - Use cautionVehicle
KZRV VENOM (2017) recall — Equipment
KZRV is recalling 2016-2018 Venom fifth-wheel trailers with outside kitchen option due to fire risk from missing copper pipe that could overheat and melt gas line.
KZRVMay 30, 2017 - UnratedDrug
Mckesson Packaging Services recalls BuPROPion HCL Tablets, USP, 75 mg, packaged as UD 100 tablets (10x10), Rx Only, Mfg by: Sandoz Inc., 508 Carnegie
Mckesson Packaging Services recalls BuPROPion HCL 75mg tablets due to moisture content exceeding specifications. Affected lots expire April 2018 or June 2018. No remedy specified in official notice.
Mckesson Packaging ServicesMay 30, 2017 - Lower riskFood
ASK Foods Inc recalls Taste of Inspirations; Greek Pasta Salad, Net Wt. 10 oz.; Distributed By: DZA Brands, LLC, Salisbury, NC
ASK Foods recalls Greek Pasta Salad (10 oz) due to possible undeclared milk. Consumers should check for incorrect nutrition labels from another product.
ASK FoodsMay 30, 2017 - Use cautionFood
Hans Kissle Company, LLC recalls Whole Foods Cranberry Couscous- packaged in Clear plastic clamshell for 6oz, 14oz and 18oz, and white plastic pail for
Whole Foods Cranberry Couscous packaged in clear plastic clamshells and white pails contains undeclared cashews. Consumers should avoid use due to tree nut allergy risk.
Hans KissleMay 28, 2017 - Lower riskMeat & poultry
Readfield Meats, Inc. Recalls Beef Trimming Products Due to Possible Adulteration
Readfield Meats recalls approximately 45,985 pounds of beef trimmings for cooking only due to possible adulteration. Products may contain foodborne pathogens if not properly processed.
Readfield MeatsMay 27, 2017 - Lower riskMeat & poultry
Cauldron Soups, LLC Recalls Beef Broth Products Produced Without Benefit of Inspection
USDA recalls 5,163 pounds of beef broth products made without federal inspection. Consumers should not consume or discard these items.
Cauldron BrothsMay 26, 2017 - Use cautionVehicle
FOREST RIVER VIBE (2017) recall — Equipment
Forest River recalls 2016-2017 Vibe trailers with incorrect tire placards that could lead to improper tire installation or underinflation, increasing crash risk. Owners must get corrected placards.
Forest RiverMay 26, 2017 - Use cautionVehicle
VANLEIGH VILANO (2018) recall — Tires
VanLeigh is recalling 2015-2018 Vilano fifth-wheel trailers due to spare tire winch not being securely fastened, which could cause the spare tire to fall off while moving, increasing crash risk. Owners should contact customer service for free fix.
VanLeighMay 26, 2017
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