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Latest recalls
35,004 found- Lower riskMedical device
Howmedica Osteonics Corp. recalls Stryker X-Change Medial Wall Mesh Small (6-Petal)-Intended to be implanted to replace a hip joint REF 0942-8-025
Howmedica recalls hip replacement mesh due to incorrect part mix-up in shipments. Affected units contain 4-petal mesh instead of 6-petal. No injury reported, but users should check their product.
HowmedicaOct 3, 2019 - Lower riskMedical device
Philips North America, LLC recalls HeartStart XL+ Defibrillator/Monitor, Model 861290
Philips recalls HeartStart XL+ Defibrillator Model 861290 that may fail to turn on or restart unexpectedly, rendering it unable to return to ready state. Affected units may not function properly during self-tests.
PhilipsOct 3, 2019 - Lower riskMedical device
Datascope Corp. recalls Low Level Output Cable Interface to Philips Monitor For Use With Cardiosave and CS300 Intra-Aortic Balloon Pumps
Datascope recalls a specific low level output cable for cardiac pumps due to incorrect cable in packaging. Affected units may have safety risks.
DatascopeOct 3, 2019 - Lower riskMedical device
Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) recalls Programmers & Remote Monitoring Software Apps: 29901 CareLink Encore Programmer
Medtronic CareLink Encore Programmer (serial numbers listed) may display inaccurate remaining battery life for some implanted cardiac devices. This does not affect device function but could lead to unexpected battery depletion. No action is required for most users.
MedtronicOct 3, 2019 - Lower riskMedical device
Cook Inc. recalls Guardia Access Nano Embryo Transfer Catheter is use for transferring IVF embryos into the uterine cavity.
Cook recalls Guardia Access Nano Embryo Transfer Catheters that may bend, causing difficulty inserting during IVF embryo transfers. Affected units may require repeat procedures or additional IV: cycles.
CookOct 3, 2019 - Use cautionMedical device
Ethicon Endo-Surgery Inc recalls ECHELON FLEX ENDOPATH 60mm Stapler - 340mm shaft, Product Code EC60A
Ethicon recalls ECHELON FLEX ENDOPATH 60mm staplers with specific product codes due to potential staple line failure causing surgery complications. Affected units may require replacement to prevent serious risks.
EthiconOct 3, 2019 - Lower riskFood
King Bottling, Inc. recalls Climax Spring Water bottled in 5 gallon, 1 gallon, and 16.9 ounce plastic bottles (12 bottles per case)
King Bottling's Climax Spring Water bottles (5 gal, 1 gal, 16.9 oz) with specific batch numbers contain bromate above FDA's 0.010 mg/L limit. Consumers should check batch numbers on bottles or caps to determine if affected.
King BottlingOct 3, 2019 - Lower riskFood
G&C Food Distributors, Inc. recalls Frozen blackberries, packaged in 16 ounce (454 gram) plastic bags (12 bags per master case). Plastic bags labeled with:
Cornerstone Premium Foods recalls frozen blackberries packaged in 16oz plastic bags contaminated with norovirus. Consumers should avoid eating these products to prevent illness.
Cornerstone Premium FoodsOct 3, 2019 - Lower riskFood
Arcadia Trading Inc. recalls Dried Mushroom NET WT: 8oz (227g) Ingredients: Mushroom Distributed By: Arcadia Trading Inc. Brooklyn, NY 11211. USA
Arcadia Trading recalls dried mushrooms (8oz) due to undeclared sulfites. This may cause allergic reactions in sensitive individuals. Consumers should check UPC 791804603091 for affected products.
Arcadia TradingOct 3, 2019 - UnratedFood
Grand Strand Sandwich Company,Inc. recalls fresh AND LOCAL CHICKEN SALAD on Croissant; Manufactured for Coremark; NET WT 6 OZ; UPC 0 67068 13105 3
Grand Strand Sandwich Company recalls chicken salad products due to possible Listeria monocytogenes contamination. Consumers should check product dates and contact the company for details.
Grand Strand SandwichOct 3, 2019 - Lower riskFood
Han Yang Corp. recalls Honey Donut (Yahk Gwa), brand name Han Yang, packaged in a white Styrofoam boat wrapped in plastic wrap, 8 pieces per
Han Yang recalls Honey Donut (Yahk Gwa) products due to undeclared wheat. Check your packages for white Styrofoam boat packaging with 8 pieces. No remedy stated in official notice.
Han YangOct 3, 2019 - Stop using nowConsumer product
VIQUA Recalls Solenoid Valve Kits for UV Water Treatment Systems Due to Electrical Shock Hazard
VIQUA recalls solenoid valve kits for UV water treatment systems due to electrical shock risk. Affected units have specific ASCO part numbers and date codes from 2018-2019. Consumers must stop using and inspect green coils for production codes.
VIQUAOct 3, 2019 - Stop using nowConsumer product
Signature Hardware Recalls Bath Stools Due to Fall and Injury Hazards (Recall Alert)
Signature Hardware recalls bath stools that can break during use, causing falls and injuries. Consumers should stop using and get a full refund.
Signature HardwareOct 3, 2019 - Stop using nowConsumer product
Ridgewood Recalls Four-Drawer Dressers Due to Tip-Over and Entrapment Hazards; Sold Exclusively at Kmart
Ridgewood recalls four-drawer dressers that can tip over or entrap children if not anchored to walls. These dressers were sold at Kmart and may cause serious injury or death.
RidgewoodOct 3, 2019 - Stop using nowConsumer product
E&E Recalls Bedroom Dressers Due to Tip-Over and Entrapment Hazards
INK+IVY Renu dressers without wall anchoring risk tipping over or entrapment, potentially causing injury or death to children. Consumers must anchor or remove these dressers to avoid hazards.
E&EOct 3, 2019 - Lower riskMedical device
Angiodynamics Inc. (Navilyst Medical Inc.) recalls Starburst Talon Semi-Flex Electrosurgical Device, Part Number H7877001028451 incorrectly labelled as Starburst MRI
Angiodynamics recalls Starburst Talon Semi-Flex Electrosurgical Devices incorrectly labeled as Starburst MRI. This labeling error may cause procedural delays for end users.
AngiodynamicsOct 2, 2019 - Lower riskMedical device
Exactech, Inc. recalls 2.4mm x 2.5 Fluted Pin Pouch; Catalog Number: 351-90-22; Orthopedic surgical instrument used in the implantation of the
Exactech recalls 2.4mm x 2.5 Fluted Pin Pouch (Catalog 351-90-22) used in ankle surgery. The pouch may contain only one pin instead of four, risking improper implantation. Affected units have specific serial numbers and packaging lots.
ExactechOct 2, 2019 - Use cautionMedical device
Zeiss, Carl Inc recalls Component for Laser Scanning Microscopes (LSM 700, LSM 800 and LSM 900)
Zeiss recalls LSM 700, 800, and 900 microscopes with certain stage stands. Tilting the light arm can bypass safety and emit class IIb laser radiation, potentially causing injury.
ZeissOct 2, 2019 - Lower riskMedical device
Medicrea International recalls Medicrea TLIF-B Holder, short intended for Intervertebral body fusion device Catalog: Number A24200010
Medicrea recalls TLIF-B Holders (Catalog A24200010) due to potential separation of inner draw rod from proximal knob. Affected units sold with Lot Numbers l9B0570 or l9B0572.
MedicreaOct 2, 2019 - Use cautionMedical device
Pega Medical Inc. recalls SCFE (slipped capital femoral epiphysis) Knobs for Driver, 6.5mm and 7.3 mm Orthopedic surgical instrument component,
Pega Medical recalls SCFE surgical knobs with potential loose screws after ultrasonic cleaning. Affected models include SCF-KNB265, SCF-KNB273, SC: 160428-03 to A183-06. Stop using immediately to prevent dislodgement.
Pega MedicalOct 2, 2019 - Use cautionDrug
Pfizer Inc. recalls 10% LMD in 5% Dextrose Injection Dextran 40 in Dextrose Injection, USP, 500 mL bags, Rx only, Hospira, Inc., Lake
Pfizer recalls 500mL Dextrose Injection bags with potential leak risk. Affected lots expire March 2020. Stop using if leaking.
PfizerOct 2, 2019 - Use cautionFood
The Great Spirits Baking Company, LLC recalls Jack Daniels Tennessee Whiskey Cake - Chocolate - Net Wt 8 OZ (227 g), UPC: 854621004349
The Great Spirits Baking Company recalls Jack Daniels Tennessee Whiskey Cake due to potential mold. Check UPC and best-by dates.
The Great Spirits Baking CompanyOct 2, 2019 - Lower riskMedical device
Aesculap Implant Systems LLC recalls Aesculap Sterile disposable fleece drape, Product code: GA414, individually packaged, 50 pieces per shipping unit,
Aesculap recalls sterile disposable fleece drapes (product code GA414) due to unverified packaging seals risking contamination. Affected units include specific lot numbers and shipping units.
AesculapOct 1, 2019 - Lower riskMedical device
Arthrex, Inc. recalls Low Profile Screw, 4.5 x 20 mm The Low Profile ScrewTM, 4.5 x 20 mm, AR-8545-20, is used with the Ankle Fusion Line of
Arthrex recalls Low Profile Screw (4.5x20mm, AR-8545-20) due to being 6mm longer than intended. This may cause improper bone fixation during ankle fusion surgery. Affected units have batch number 10308261.
ArthrexOct 1, 2019 - UnratedMedical device
Monarch Medical Technologies recalls EndoTool SubQ (Versions 1.7.1, 1.7.4, 1.7.5)
Monarch Medical Technologies recalls EndoTool SubQ versions 1.7.1, 1.7.4, and 1.7.5 due to distribution before FDA approval. Affected users should contact the company for details.
Monarch Medical TechnologiesOct 1, 2019 - Lower riskMedical device
Mindray DS USA, Inc. dba Mindray North America recalls Accutorr 3 Vital Signs Monitor with NIBP valve assembly board, p/n 115-017679-00, containing software version 8.1.5 -
Mindray recalls Accutorr 3 Vital Signs Monitors with specific software version 8.1.5 that may have NIBP valve assembly problems. Affected units could have unapproved software features that might cause hose blockages.
MindrayOct 1, 2019 - Lower riskMedical device
Bard Peripheral Vascular Inc recalls BardPort M.R.I. Hard Base Implantable Port with Attachable 9.6 F Open-Ended Single-Lumen Venous Catheter, Ref: 0604550,
Bard recalls specific implantable ports that may contain incorrect catheter tips, potentially prolonging surgery. Affected units include those with reference number 0604550 and lot number RECR1431.
BardOct 1, 2019 - Stop using nowDrug
New Vitalis Pharmacy LLC dba New Vitalis Pharmacy recalls Testosterone Cypionate 180 mg/mL/Testosterone Propionate 20mg/mL Oil Injection Solution, 10 mL per vial, New Vitalis
New Vitalis Pharmacy recalls testosterone injections with lot numbers AL-07232019 to AL-09032019 due to lack of sterility assurance. Consumers should not use these products.
New Vitalis PharmacyOct 1, 2019 - Lower riskDrug
Sato Pharmaceutical Inc. recalls Sankaijo BOTANICAL LAXATIVE (docusate sodium 8.33 mg and sennosides 1.36 mg) tablets, 150-count bottles, Manufactured
Sato Pharmaceutical recalls 150-count laxative tablets with less than labeled sennosides. This may not provide expected bowel movement relief. Consumers should check lot numbers and contact the company for details.
Sato PharmaceuticalOct 1, 2019 - Stop using nowDrug
Dr. Reddy's Laboratories, Inc. recalls Ranitidine Tablets, USP 150 mg, a.) 65 count bottles (NDC 49035-404-61) b.) 130 count bottles (NDC 49035-404-13) c.)
Dr. Reddy's recalls 150mg ranitidine tablets with NDMA impurity detected. Stop using affected batches to avoid potential health risks.
Dr. Reddy'sOct 1, 2019
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