The Recall Desk

Archive

January 2017 recalls

913 recalls were announced in January 2017.

What the numbers show

Critical
104
Severe
443
High
205
Moderate
130
Low
31

Of the 913 recalls this month scored against our rubric, 11% are Critical, 49% are Severe.

Which agencies issued them

301–400 of 913

  • HighFDA (Food)·F-1234-2017·2017-01-18

    Fourth Street Barbecue Recalls Macaroni and Cheese Due to Salmonella Risk

    Fourth Street Barbecue is voluntarily recalling specific macaroni and cheese products because the powdered cheese packets may contain milk powder contaminated with Salmonella.

    Product
    Cardboard sleeve: Double Takes Macaroni & Cheese Dinner, Distributed By: Greenbrier International, Inc., 500 Volvo Parkway, Chesapeake, VA 23320; Double Takes: Best By: 10/11/17 10/12/17 10/13/17 10/19/17 10/20/17 10/24/17 11/28/17 11/29/17 11/30/17; UPC: 63927701208:
    Category
    Food
    Distribution
    10 states
  • HighFDA (Food)·F-1094-2017·2017-01-18

    Piazza Produce Garden Season No Salt Recalled for Undeclared Soybean Oil

    Piazza Produce is recalling Garden Season No Salt products because the labels do not list soybean oil as an ingredient.

    Product
    Garden season no salt, 5 lb plastic gallon, product number 63516; Garden season no salt, 1.25 lb plastic jar, product number 63514
    Category
    Food
    Distribution
    5 states
  • HighFDA (Devices)·Z-0990-2017·2017-01-18

    Varian Eclipse Treatment Planning System Software Recall for Contouring Errors

    Varian Medical Systems is recalling 42 Eclipse Treatment Planning System devices due to a software defect that prevents contours from saving consistently.

    Product
    Eclipse Treatment Planning System version 13.MR2 [13.06.31 with Smart Segmentation Knowledge Based Contouring version 2.3 [2.3.12] Radiology: The Eclipse Treatment Planning System (Eclipse TPS) is used to plan radiotherapy treatments for patients with malignant or benign d
    Category
    Medical Device
    Distribution
    4 states
  • HighFDA (Devices)·Z-0987-2017·2017-01-18

    Elekta Oncentra Radiation Therapy Software Recalled for Cross Profile Defect

    Elekta, Inc. is recalling Oncentra External Beam and Brachy software because a cross profile for a Varian 60-degree wedge shows 'horns.' The recall covers 433 units distributed worldwide.

    Product
    Oncentra External Beam Oncentra Brachy Product Usage: Oncentra is radiation therapy planning software designed to analyze and plan radiation treatment is three dimensions for the purpose of treating patients with cancer.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0862-2017·2017-01-18

    Koi Palace Mini Moon Cakes Recalled for Undeclared Allergens

    Magic Gourmet Trading Inc. is recalling Koi Palace Mini Moon Cakes because they lack adequate labeling and contain undeclared allergens.

    Product
    Koi Palace Mini Moon Cake: Dalmaji with Happy Family Unit Size 1/2 lb. and 1/4 lb. in circular box (1 piece) and rectangular boxes (4, 6 or 8 pieces).
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·F-1189-2017·2017-01-18

    Valley Milk Products Recalls Non Fat Dry Milk for Salmonella Risk

    Valley Milk Products is recalling Non Fat Dry Milk due to potential Salmonella contamination. The product was distributed to brokers and direct accounts in multiple states.

    Product
    Non Fat Dry Milk, Grade A - High Heat in 50 # bags , manufactured by Valley Milk Products. Stasburg, Virginia 22657 , Permit No. 51-4136 Net Weight - 50 LBS
    Category
    Food
    Distribution
    10 states
  • HighFDA (Food)·F-1218-2017·2017-01-18

    Stonewall Kitchen Orange Cranberry Pancake Mix Recalled for Salmonella Risk

    Stonewall Kitchen is recalling 40 units of Orange Cranberry Pancake & Waffle Mix due to potential salmonella contamination. The product was distributed in six states.

    Product
    Stonewall Kitchen Orange Cranberry Pancake & Waffle Mix, Packaged in a 16oz. canister UPC: 711381325971 Item #: 554130
    Category
    Food
    Distribution
    6 states
  • HighFDA (Food)·F-1206-2017·2017-01-18

    All American Seasonings Recalls Guy's Sour Cream & Cheddar Chip Seasoning

    All American Seasonings, Inc. is recalling 12 boxes of Guy's Sour Cream & Cheddar Chip Seasoning due to potential Salmonella contamination.

    Product
    Guy's Sour Cream & Cheddar Chip Seasoning. Product Code: T3040A. 50 lb box
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1217-2017·2017-01-18

    Stonewall Kitchen Cinnamon Apple Pancake Mix Recalled for Salmonella Risk

    Stonewall Kitchen is recalling Cinnamon Apple Pancake & Waffle Mix due to potential Salmonella contamination. Consumers should stop using the product.

    Product
    Stonewall Kitchen Cinnamon Apple Pancake & Waffle Mix, 16 oz. canister UPC: 711381025659 Item #: 551118
    Category
    Food
    Distribution
    6 states
  • ModerateFDA (Devices)·Z-0992-2017·2017-01-18

    Siemens Biograph mCT PET/CT Scanner Laser Cover Window Recall

    Siemens is recalling 41 Biograph mCT PET/CT scanners because laser cover windows may fall off.

    Product
    Biograph mCT S(40)-3R, Material Number 10248668 The Siemens Biograph mCT and Biograph mCT Flow systems are combined X-Ray Computed Tomography (CT) and Positron Emission Tomography (PET) scanners that provide registration and fusion of high resolution physiologic and anatomic in
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0982-2017·2017-01-18

    Bard Access Systems Recalls StatLock Catheter Stabilization Devices

    Bard Access Systems is voluntarily recalling StatLock CV Plus catheter stabilization devices because some pouches lack unique product identifiers.

    Product
    StatLock¿ CV Plus w/Pigtail. Product Code: CV0220CE & CV0220. Packaged as a single unit with a skin protectant pad and foam strips in a Tyvek pouch. Depending on configuration, there are either 25 or 50 pouches per carton and 10 cartons per case. Other configurations may contain
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0973-2017·2017-01-18

    GE Healthcare Recalls OEC 9800 Imaging Systems Due to Power Cable Failures

    GE Healthcare is conducting a voluntary field action for OEC 9800 systems because the workstation power cable assembly can cause intermittent power cord failures.

    Product
    OEC 9800. MDL Numbers: D222250, D141598 The OEC 9800 is designed to provide fluoroscopic and spot-film imaging of the patient during diagnostic, surgical and interventional procedures. Clinical application may include cholangiography, endoscopy, urologic, orthopedic, neurologic,
    Category
    Medical Device
    Distribution
    50 states
  • ModerateFDA (Devices)·Z-0983-2017·2017-01-18

    Bausch & Lomb Recalls Algerbrush-II Ophthalmic Surgical Instruments

    Bausch & Lomb is recalling Algerbrush-II surgical instruments because some units shipped with outdated operating instructions.

    Product
    Algerbrush-II Product Usage: Medical - For surgeons to use in ophthalmic surgical procedures to remove foreign bodies from the eye of the patient
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateUSDA FSIS·006-2017·2017-01-18

    Burgers Ozark Country Cured Recalls Mislabeled Turkey Products

    Burgers Ozark Country Cured is recalling approximately 1,905 pounds of fully cooked turkey products due to misbranding. The products contain undeclared sodium nitrite.

    Product
    Burger's Ozark Country Cured Hams, Inc. — Burgers Ozark Country Cured Recalls Poultry Products Due To Misbranding
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0954-2017·2017-01-18

    In2Bones Recalls NEOVIEW Screws Due to Thread Dimensional Non-Conformity

    In2Bones is recalling 26 units of NEOVIEW Screws Set due to dimensional non-conformity of the thread on the screw head.

    Product
    NEOVIEW(R) SCREWS SET, REF W27 ST900, STERILE R The NEOVIEW¿ Plating System is intended for fixation of intra-articular and extraarticular fractures of the distal radius and reconstruction of the distal radius
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-0974-2017·2017-01-18

    GE OEC MiniView 6800 C-Arm Recalled for Power Cable Failures

    GE Healthcare is conducting a voluntary field action for OEC MiniView 6800, OEC 9900 Elite, and OEC 9800 devices due to intermittent power cord failures.

    Product
    OEC MiniView 6800. MDL Number: D002533 The OEC MiniView 6800 Digital Mobile C-Arm is designed to provide the physician with general fluoroscopic visualization of the patient including but not limited to surgical orthopedic and extremity imaging. The device is not intended for wh
    Category
    Medical Device
    Distribution
    50 states
  • ModerateFDA (Food)·F-1244-2017·2017-01-18

    H-E-B Recalls White Corn Tortillas Due to Foreign Material

    H-E-B is recalling specific lots of Homestyle White Corn Tortillas because they may contain foreign material, possibly corn husk.

    Product
    HEB Homestyle White Corn Tortillas, 12 Count and 30 Count packaged in clear plastic bags.
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Food)·F-1089-2017·2017-01-18

    Piazza Produce Recalls Cajun Seasoning for Missing Ingredient Labeling

    Piazza Produce, Inc. is recalling three sizes of Cajun seasoning because the product labels do not list ingredients. The recall affects food service establishments in five states.

    Product
    Cajun seasoning, 5.5 lb plastic gallon, product number 61798; Cajun seasoning, 1.5 lb plastic jar, product number 61779; Cajun seasoning, 12 lb plastic pail, product number 61817
    Category
    Food
    Distribution
    5 states
  • ModerateFDA (Food)·F-1091-2017·2017-01-18

    Piazza Produce Recalls Chili Powder for Missing Ingredient Labeling

    Piazza Produce, Inc. is recalling various sizes of chili powder because the product labeling does not contain a listing of ingredients.

    Product
    Chili Powder, 5 lb plastic gallon, product number 62235; Chili Powder, 1.25 lb plastic jar, product number 62216; Chili Powder, 10 lb plastic pail, product number 62254; Chili Powder, 22 lb plastic pail, product number 62273
    Category
    Food
    Distribution
    5 states
  • ModerateFDA (Devices)·Z-0993-2017·2017-01-18

    Siemens Biograph mCT Scanners Recalled for Falling Laser Cover Windows

    Siemens is recalling 34 Biograph mCT scanners because laser cover windows may fall off, posing a potential hazard to users.

    Product
    Biograph mCT S(64)-3R, Material Number 10248669 The Siemens Biograph mCT and Biograph mCT Flow systems are combined X-Ray Computed Tomography (CT) and Positron Emission Tomography (PET) scanners that provide registration and fusion of high resolution physiologic and anatomic in
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0952-2017·2017-01-18

    In2Bones Recalls 19 Locking Screws Due to Thread Dimensional Non-Conformity

    In2Bones is recalling 19 locking screws from the NEOVIEW Plating System due to dimensional non-conformity of the thread on the screw head.

    Product
    SCREW 02.7-12MM LOCKING, REF W27 ST112: a) DRP, b) NEO, In2Bones, 28 chemin du petit bois, 69130 Ecully - France The NEOVIEW¿ Plating System is intended for fixation of intra-articular and extraarticular fractures of the distal radius and reconstruction of the distal radius
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-0999-2017·2017-01-18

    Siemens Biograph mCT-X Scanner Recall Due to Falling Laser Cover Windows

    Siemens Medical Solutions is recalling Biograph mCT-X scanners because laser cover windows may fall off.

    Product
    Biograph mCT-X w/TrueV Upgrade, Material Number 10250745 The Siemens Biograph mCT and Biograph mCT Flow systems are combined X-Ray Computed Tomography (CT) and Positron Emission Tomography (PET) scanners that provide registration and fusion of high resolution physiologic and an
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0958-2017·2017-01-18

    Straumann Twist Drill PRO Recalled for Tolerance Specification Defects

    Straumann Manufacturing is recalling 120 units of Twist Drill PRO dental implant accessories because they cannot be inserted into handpieces due to tolerance specification failures.

    Product
    Straumann Twist Drill PRO ¿4.2mm,long,41mm,SS-Non sterile. Dental implant accessory Article Number: 044.255 Dental implants drill accessory is intended to prepare osteotomy site for surgical dental implant placement. Dental implants are intended for immediate placement and f
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1097-2017·2017-01-18

    Piazza Produce Recalls Herb De Provence for Missing Ingredient Labeling

    Piazza Produce is recalling Herb De Provence in three sizes because the product labels do not list ingredients. The recall affects food service establishments in five states.

    Product
    Herb De Provence, 1.25 lb plastic gallon, product number 64477; Herb De Provence, 6 oz plastic jar, product number 64458; Herb De Provence, 3 lb plastic pail, Product code 64496
    Category
    Food
    Distribution
    5 states
  • ModerateFDA (Food)·F-1179-2017·2017-01-18

    Starkey Spring Water Recalled Due to Arsenic Detection

    Starkey Water is recalling 16.9 fl oz glass bottles of Starkey Spring Water because 11.7 ppb of arsenic was detected in a water sample.

    Product
    Starkey Spring Water, Item code STC.5, 16.9 FL oz. (500 mL) glass bottle. Product UPC 8 11904 02000 7. Case UPC 8 11904 02002 1.
    Category
    Food
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-0427-2017·2017-01-18

    Pharm D Solutions Recalls HCG-Vitamin B12 Injection Due to Labeling Error

    Pharm D Solutions is recalling 112 vials of HCG-Vitamin B12 injection because the product description incorrectly states the HCG strength as 7500 units instead of 5000 units.

    Product
    HCG-Vitamin B12 5000 IU-8 mg in 10 mL vial, Rx only, For Sub-Q & IM Injection, Pharm D Solutions, Loop West Houston, TX --- NDA 69699-1723-20
    Category
    Drug
    Distribution
    2 states
  • ModerateFDA (Devices)·Z-0994-2017·2017-01-18

    Siemens Biograph mCT X-4R Laser Cover Window Recall

    Siemens is recalling 71 Biograph mCT X-4R scanners because laser cover windows may fall off.

    Product
    Biograph mCT X-4R, Material Number 10248670 The Siemens Biograph mCT and Biograph mCT Flow systems are combined X-Ray Computed Tomography (CT) and Positron Emission Tomography (PET) scanners that provide registration and fusion of high resolution physiologic and anatomic inform
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0980-2017·2017-01-18

    ICU Medical Recalls 24-Hour Primary Sets with Incorrect Drip Chambers

    ICU Medical is recalling 225 units of 24-hour primary sets where a 15-drop drip chamber was installed instead of the required 60-drop chamber.

    Product
    133" 60 Drop 24 Hour Primary Set w/2 Bravo24¿, 2 Gang 1o2¿ Manifold, Rotating Luer, 1 Ext, Item No. B59006 Product Usage: The intravascular administration set is a single use, sterile, non-pyrogenic device which provides access for the administration of fluids from a containe
    Category
    Medical Device
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-0959-2017·2017-01-18

    Brainlab Knee Navigation Cutting Block Adapter Base Recalled for Material Error

    Brainlab AG is recalling specific femoral and tibial cutting block adapter bases because they may contain incorrect material, making them unsuitable for reprocessing.

    Product
    Femoral and Tibial Cutting Block Adapter Base. Brainlab knee, BrainLAB Image Guided Surgery System / Instrument, Stereotaxic
    Category
    Medical Device
    Distribution
    4 states
  • ModerateFDA (Devices)·Z-1000-2017·2017-01-18

    Siemens Biograph mCT 20 Excel PET/CT Scanner Recall for Laser Cover Windows

    Siemens is recalling 51 Biograph mCT 20 Excel scanners because laser cover windows may fall off.

    Product
    BIOGRAPH mCT 20 Excel, Material Number 10507786 The Siemens Biograph mCT and Biograph mCT Flow systems are combined X-Ray Computed Tomography (CT) and Positron Emission Tomography (PET) scanners that provide registration and fusion of high resolution physiologic and anatomic in
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0961-2017·2017-01-18

    Implant Direct Recalls GoDirect Screw-Retaining Top Due to Labeling Error

    Implant Direct Sybron Manufacturing is recalling 14 units of GoDirect Screw-Retaining Top (Part No. 4500-61) because they were shipped with incorrect labels for a different product.

    Product
    GoDirect Screw-Retaining Top Part Numbers: 4500-61
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-0998-2017·2017-01-18

    Siemens Biograph mCT PET/CT Scanner Laser Cover Window Recall

    Siemens Medical Solutions is recalling Biograph mCT PET/CT scanners because laser cover windows may fall off.

    Product
    Bio mCT-S(40) 3R->4R Upgrade, Material Number 10250743 The Siemens Biograph mCT and Biograph mCT Flow systems are combined X-Ray Computed Tomography (CT) and Positron Emission Tomography (PET) scanners that provide registration and fusion of high resolution physiologic and anat
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1016-2017·2017-01-18

    Hospira Recalls Minibore Extension Sets Due to Solvent Occlusion

    Hospira is voluntarily recalling one lot of Minibore Extension Sets due to a confirmed report of solvent occlusion that may prevent priming and delay therapy.

    Product
    Minibore Extension Set, 59 Inch with Spin Lock Collar, Non-DEHP, Latex-Free Intended use: For the administration of drugs and solutions to a patient's vascular system through a vascular access device.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0986-2017·2017-01-18

    Bard Access Systems Recalls SafeStep Huber Needle Sets Due to Labeling Errors

    Bard Access Systems is recalling SafeStep Huber Needle Sets because some units may have needle lengths or gauges that differ from the label.

    Product
    SafeStep¿ Huber Needle Set with Y-Injection Site. Product Code: LH-0029YN. Packaged as single units in thermoformed trays. There are 25 SafeStep¿ trays per case and 100 per carton. Product Usage: Intended for the administration of fluids and drugs, or blood sampling through s
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1092-2017·2017-01-18

    Piazza Produce Recalls Curry Powder for Missing Ingredient Labeling

    Piazza Produce, Inc. is recalling two sizes of curry powder because the product labeling does not contain a listing of ingredients.

    Product
    Curry Powder, 4.25 lb plastic gallon, product number 63375; Curry Powder, 1 lb plastic jar, product number 63356
    Category
    Food
    Distribution
    5 states
  • ModerateFDA (Devices)·Z-0996-2017·2017-01-18

    Siemens Biograph mCT PET/CT Scanners Recalled for Falling Laser Cover Windows

    Siemens Medical Solutions is recalling 102 Biograph mCT PET/CT scanners because laser cover windows may fall off.

    Product
    Biograph mCT S(64)-4R, Material Number 10248672 The Siemens Biograph mCT and Biograph mCT Flow systems are combined X-Ray Computed Tomography (CT) and Positron Emission Tomography (PET) scanners that provide registration and fusion of high resolution physiologic and anatomic in
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1001-2017·2017-01-18

    Siemens Biograph mCT Flow Edge-4R Scanner Recall for Laser Cover Windows

    Siemens Medical Solutions is recalling one Biograph mCT Flow Edge-4R scanner because laser cover windows may fall off.

    Product
    Biograph mCT Flow Edge-4R, Material Number 10528955 The Siemens Biograph mCT and Biograph mCT Flow systems are combined X-Ray Computed Tomography (CT) and Positron Emission Tomography (PET) scanners that provide registration and fusion of high resolution physiologic and anatomi
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0425-2017·2017-01-18

    Baxter Recalls Premasol Sulfite-Free Amino Acid Injection Due to Discoloration

    Baxter Healthcare is recalling 3,528 units of Premasol Sulfite-Free Amino Acid Injection due to yellow discoloration caused by a damaged overpouch.

    Product
    PREMASOL - SULFITE-FREE (AMINO ACID) — PREMASOL - SULFITE-FREE (AMINO ACID) (LEUCINE, LYSINE, ISOLEUCINE, VALINE, HISTIDINE, PHENYLALANINE, THREONINE, METHIONINE, TRYPTOPHAN, TYROSINE, N-ACETYL-TYROSINE, ARGININE, PROLINE, ALANINE, GLUTAMIC ACIDE, SERINE, GLYCINE, ASPARTIC ACID, TAURINE, CYSTEINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    0 states
  • ModerateFDA (Food)·F-1245-2017·2017-01-18

    Fabi-saa Melcochas Candy Recalled Due to Undeclared Yellow #5 Dye

    Fabi-saa Inc. is recalling Melcochas Candy because analysis revealed the presence of Yellow #5 dye, which was not declared on the label.

    Product
    Fabi-saa Melcochas Candy Net Wt. 8 oz. Fabi-Saa Inc. 39 Montgomery Street Belleville, NJ 07936 UPC 181683000676
    Category
    Food
    Distribution
    2 states
  • ModerateFDA (Devices)·Z-0957-2017·2017-01-18

    Straumann Dental Implant Drills Recalled for Tolerance Specification Failures

    Straumann Manufacturing is recalling 165 dental implant drills because they cannot be inserted into handpieces due to tolerance specification failures.

    Product
    Straumann Drill 1, short, ¿ 2.2mm, l 33.0mm, SS-Non sterile. Dental implant accessory Article Number: 044.210 Dental implants drill accessory is intended to prepare osteotomy site for surgical dental implant placement. Dental implants are intended for immediate placement and
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0981-2017·2017-01-18

    Bard Access Systems Recalls StatLock PICC Plus Devices Due to Missing Identifiers

    Bard Access Systems is recalling StatLock PICC Plus Crescent Foam devices because some pouches lack unique product identifiers like lot numbers.

    Product
    StatLock¿ PICC Plus Crescent Foam. Product Code: VPPCSP & VPPCSPCE. Packaged as a single unit with a skin protectant pad and foam strips in a Tyvek pouch. Depending on configuration, there are either 25 or 50 pouches per carton and 10 cartons per case. Other configurations may co
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1019-2017·2017-01-18

    Acumed Recalls OPT Croutons Synthetic Bone Substitute Due to Sterilization Documentation Issues

    Acumed LLC is recalling 83 units of OPT Croutons synthetic bone substitute because documentation for the sterilization dose was inadequate. The product was distributed in ten US states and Puerto Rico.

    Product
    OPT Croutons is a synthetic bone substitute designed for the repair of bony defects and is made of pure beta-tricalcium phosphate. The tricalcium phosphate is a soluble calcium phosphate salt.
    Category
    Medical Device
    Distribution
    9 states
  • ModerateFDA (Devices)·Z-0955-2017·2017-01-18

    VOCO Futurabond M+ adhesive recalled for labeling mix-up

    Voco GmbH is recalling 50 units of VOCO Futurabond M+ adhesive due to a labeling error where the product was marked as Futurabond M+ Universal Adhesive.

    Product
    VOCO Futurabond M+ adhesive, RF 1515, Manufactured by VOCO GmbH, Futurabond M+ is a dental adhesive for use with methacrylate-based restorative, core build-up or luting materials. It can be applied with phosphoric acid etching (selective enamel etching or total-etch) of the denta
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0975-2017·2017-01-18

    GE OEC Mobile Fluoroscopy Systems Recalled for Power Cable Failures

    GE Healthcare is recalling OEC 9900 Elite and other mobile fluoroscopy systems because the workstation power cable assembly can fail intermittently.

    Product
    The OEC 9900 Elite mobile fluoroscopy system is designed to provide fluoroscopic and spot-film images of the patient during diagnostic surgical and interventional procedure. Examples of clinical application may include cholangiography, endoscopy, urologic, orthopedic, neurologic,
    Category
    Medical Device
    Distribution
    50 states
  • ModerateFDA (Devices)·Z-0965-2017·2017-01-18

    ASP Recalls EVOTECH Endoscope Cleaner Due to Hose Leak Risk

    Advanced Sterilization Products is recalling 107 EVOTECH Endoscope Cleaner and Reprocessor Systems because a hose may come loose and cause a leak.

    Product
    EVOTECH Endoscope Cleaner and Reprocessor System 208V, Product Code: 50004 The EVOTECH ECR Endoscope Cleaner and Reprocessor, a washer/disinfector, is indicated for use with high-level disinfectant CIDEX OPA Concentrate Solution and an enzymatic detergent (CIDEZYME XTRA) to ac
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0960-2017·2017-01-18

    Trilliant Tiger Screw Sterilization Tray Base Assembly Recall for Printing Error

    Trilliant Surgical Ltd. is recalling Tiger Screw Sterilization Tray Base Assemblies due to a printing error on k-wire description markings.

    Product
    Tiger Screw Sterilization Tray Base Assembly Model 210-00-001 Revision N, O The product is a component of a system indicated for the fixation of fractures, non-unions, arthrodeses, and osteotomies of bones appropriate for the size of the device.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0991-2017·2017-01-18

    ConforMIS iTotal PS Knee Implant Recalled for Software Measurement Error

    ConforMIS is recalling iTotal PS Knee Replacement Kits because the iView software displayed femoral cut measurements in the wrong unit.

    Product
    ConFORMIS ITOTAL PS-IPOLYIMPLANT KIT-RIGHT Catalog Number:TPS-111-1111 The iTotal¿ PS Knee Replacement System is intended for use as a total knee replacement in patients with knee joint pain and disability whose conditions cannot be solely addressed by the use of a prosthetic
    Category
    Medical Device
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-0997-2017·2017-01-18

    Siemens Biograph mCT X-3R Scanners Recalled for Falling Laser Cover Windows

    Siemens Medical Solutions is recalling 18 Biograph mCT X-3R scanners because laser cover windows may fall off.

    Product
    Biograph mCT X-3R, Material Number 10248673 The Siemens Biograph mCT and Biograph mCT Flow systems are combined X-Ray Computed Tomography (CT) and Positron Emission Tomography (PET) scanners that provide registration and fusion of high resolution physiologic and anatomic inform
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0985-2017·2017-01-18

    Bard Access Systems Recalls MiniLoc Safety Infusion Sets Due to Labeling Errors

    Bard Access Systems is recalling MiniLoc Safety Infusion Sets because some units have needle lengths and gauges that differ from the label descriptions.

    Product
    MiniLoc¿ Safety Infusion Set Winged without Y-Injection Site. Product Code: S02022-75. Packaged as single units in thermoformed trays. There are 20 MiniLoc¿ trays per case and 160 per carton. Product Usage: Intended for the administration of fluids and drugs, or blood samplin
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0979-2017·2017-01-18

    Siemens Recalls Intact PTH Assay Kits Due to Negative Bias

    Siemens is recalling IMMULITE 2000 Intact PTH assay kits because they may show a negative bias of up to -39% at low concentrations.

    Product
    SIEMENS IMMULITE 2000/2000 Xpi Systems Intact PTH (Parathyroid Hormone) Test Code iPTH, REF/Catalog Number L2KPP2, Siemens Material Number (SMN) 10381441 and REF/Catalog Number L2KPP6, SMN 10381442; IVD --- Made in UK -- Siemens healthcare Diagnostics Products Ltd. Glyn Rhonw
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1002-2017·2017-01-18

    Siemens Biograph mCT Flow 40-4R Laser Cover Window Recall

    Siemens Medical Solutions is recalling Biograph mCT Flow 40-4R scanners because laser cover windows may fall off.

    Product
    Biograph mCT Flow 40-4R, Material Number 10529159 The Siemens Biograph mCT and Biograph mCT Flow systems are combined X-Ray Computed Tomography (CT) and Positron Emission Tomography (PET) scanners that provide registration and fusion of high resolution physiologic and anatomic
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0995-2017·2017-01-18

    Siemens Biograph mCT Scanners Recalled for Falling Laser Cover Windows

    Siemens Medical Solutions is recalling 88 Biograph mCT scanners because laser cover windows may fall off.

    Product
    Biograph mCT S(40)-4R, Material Number 10248671 The Siemens Biograph mCT and Biograph mCT Flow systems are combined X-Ray Computed Tomography (CT) and Positron Emission Tomography (PET) scanners that provide registration and fusion of high resolution physiologic and anatomic in
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0429-2017·2017-01-18

    Noven Recalls Daytrana Patches Due to Defective Delivery System

    Noven Pharmaceuticals is recalling Daytrana (methylphenidate) transdermal patches because the delivery system failed to meet mechanical specifications.

    Product
    DAYTRANA — DAYTRANA (METHYLPHENIDATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1017-2017·2017-01-18

    Merge Eye Station Software Recalled for Potential Data Deletion

    Merge Healthcare is recalling Merge Eye Station software versions 11.6.0 and prior due to a risk of accidental patient record deletion.

    Product
    Merge Eye Station f/k/a: DFC-1024 & DFC-512 Digital Imaging System, WinStation, and WinStation Retinal Imager distributed by Ophthalmic Imaging Systems (OIS). Versions: 11.6.0 and prior
    Category
    Medical Device
    Distribution
    52 states
  • ModerateFDA (Devices)·Z-0971-2017·2017-01-18

    Siemens Artis zee/zeego Angiographic X-ray System Recall for Generator Defects

    Siemens is recalling Artis zee/zeego angiographic x-ray systems due to potential high-voltage generator failures and rare image display loss.

    Product
    Artis zee/zeego, Angiographic x-ray system Stand alone system The Artis systems are a family of dedicated angiography systems developed for single and biplane diagnostic imaging and interventional procedures including, but not limited to, pediatric and obese patients. Procedure
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Food)·F-1096-2017·2017-01-18

    Piazza Produce Garlic Salt Recalled for Missing Ingredient Labeling

    Piazza Produce, Inc. is recalling various sizes of Garlic Salt because the product labeling does not contain a listing of ingredients.

    Product
    Garlic Salt, 9 lb plastic gallon, product number 64078; Garlic Salt, 2.5 lb plastic jar, product number 64059; Garlic Salt, 20 lb plastic pail, Product code 64097; Garlic Salt, 34 lb plastic pail, Product code 64116
    Category
    Food
    Distribution
    5 states
  • LowFDA (Food)·F-1102-2017·2017-01-18

    Piazza Produce Recalls Onion Salt for Missing Ingredient Labeling

    Piazza Produce, Inc. is recalling onion salt in various sizes because the product labeling does not contain a listing of ingredients.

    Product
    Onion salt, 9 lb plastic gallon, product number 65845; Onion salt, 2.5 lb plastic jar, product number 65826; Onion salt, 20 lb plastic pail, product number 65864
    Category
    Food
    Distribution
    5 states
  • LowFDA (Food)·F-1090-2017·2017-01-18

    Piazza Produce Recalls Celery Salt for Missing Ingredient Labeling

    Piazza Produce, Inc. is recalling celery salt products because the packaging does not list ingredients. The recall affects food service establishments in five states.

    Product
    Celery salt, 8 lb plastic gallon, product number 62064; Celery salt, 2 lb plastic jar, product number 62045; Celery salt, 16 lb plastic pail, product number 62083
    Category
    Food
    Distribution
    5 states
  • LowFDA (Drugs)·D-0426-2017·2017-01-18

    Testosterone Cypionate Injection Recalled for Incorrect Excipient Labeling

    Pharm D Solutions is recalling Testosterone Cypionate 200 mg/mL vials because the label incorrectly lists grapeseed oil instead of sesame oil.

    Product
    Testosterone Cypionate 200 mg/mL in Sesame Oil, 4 mL and 5 mL vials, Rx only, For IM injection, Pharm D Solutions, Loop West Houston, TX --- NDA 69699-1709-04
    Category
    Drug
    Distribution
    2 states
  • LowFDA (Drugs)·D-0424-2017·2017-01-18

    Pfizer Recalls Cytotec Tablets Due to Failed Impurity Specifications

    Pfizer is recalling 1,706 cartons of Cytotec (misoprostol) tablets nationwide because the product failed impurity and degradation specifications.

    Product
    CYTOTEC — CYTOTEC (MISOPROSTOL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1004-2017·2017-01-18

    Philips Brilliance iCT CT System Recalled for Undocumented Installation

    Philips Medical Systems is recalling one Brilliance iCT system because the installation of four M12 bolts was not correctly documented.

    Product
    Brilliance iCT Product Usage: Computed Tomography X-ray systems intended to produce cross-sectional Images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes. These devices may include signal analysts and display equipment,
    Category
    Medical Device
    Distribution
    0 states
  • LowFDA (Food)·F-1088-2017·2017-01-18

    Piazza Produce Recalls Blackened Seasoning for Missing Ingredient Labeling

    Piazza Produce, Inc. is recalling 715 units of blackened seasoning because the product labels do not list ingredients. The recall covers food service establishments in five states.

    Product
    Blackened seasoning, 5.5 lb plastic gallon, product number 61703; Blackened seasoning, 1.5 lb plastic jar, product number 61684; Blackened seasoning, 10 lb plastic pail, product number 61722
    Category
    Food
    Distribution
    5 states
  • LowUSDA FSIS·007-2017·2017-01-18

    Willow Tree Poultry Farm Recalls Misbranded Chicken Salad Products

    Willow Tree Poultry Farm is recalling 204 pounds of chicken salad products because they are misbranded as chicken salad but contain egg salad.

    Product
    WILLOW TREE POULTRY FARM, INC. — Willow Tree Poultry Farm, Inc. Recalls Chicken Salad Products Due To Misbranding
    Category
    Food
    Distribution
    Distributed nationwide
  • LowFDA (Food)·F-1103-2017·2017-01-18

    Piazza Produce Recalls Pumpkin Pie Spice for Missing Ingredient Labeling

    Piazza Produce, Inc. is recalling 197 units of pumpkin pie spice because the product labeling does not contain a listing of ingredients.

    Product
    Pumpkin pie spice, 4 lb plastic gallon, product number 67644; Pumpkin pie spice, 1 lb plastic jar, product number 67642
    Category
    Food
    Distribution
    5 states
  • LowFDA (Food)·F-1098-2017·2017-01-18

    Piazza Produce Recalls Hickory Smoke Salt for Missing Ingredient Labeling

    Piazza Produce is recalling 283 units of Hickory Smoke salt because the product labeling does not contain a listing of ingredients.

    Product
    Hickory Smoke salt, 7.5 lb plastic gallon, product number 64527; Hickory Smoke salt, 2.25 lb plastic jar, product number 64553; Hickory Smoke salt, 15 lb plastic pail, Product code 64591
    Category
    Food
    Distribution
    5 states
  • LowFDA (Food)·F-1087-2017·2017-01-18

    Piazza Produce Recalls BBQ Spice for Missing Ingredient Labeling

    Piazza Produce, Inc. is recalling specific lots of BBQ Spice because the product labeling does not contain a listing of ingredients.

    Product
    BBQ Spice, 6 lb plastic gallon, product number 61608; BBQ Spice, 1.75 lb plastic jar, product number 61589; BBQ Spice, 15 lb plastic pail, product number 61627
    Category
    Food
    Distribution
    5 states
  • LowFDA (Food)·F-1106-2017·2017-01-18

    Piazza Produce Recalls Seafood Seasoning for Missing Ingredient Labeling

    Piazza Produce, Inc. is recalling seafood seasoning products because the labels do not list ingredients. This affects food service establishments in five states.

    Product
    Seafood seasoning, 5 lb plastic gallon, product number 68296; Seafood seasoning, 1.25 lb plastic jar, product number 68277; Seafood seasoning, 10 lb plastic pail, product number 68315
    Category
    Food
    Distribution
    5 states
  • LowFDA (Food)·F-1108-2017·2017-01-18

    Piazza Produce Recalls Taco Seasoning for Missing Ingredient Labeling

    Piazza Produce, Inc. is recalling 701 units of taco seasoning because the product labeling does not contain a listing of ingredients.

    Product
    Taco seasoning, 5.5 lb plastic gallon, product number 68667; Taco seasoning, 1.5 lb plastic jar, product number 68665
    Category
    Food
    Distribution
    5 states
  • SevereNHTSA·17V037000·2017-01-17

    Highland Ridge RV Recalls 2017 Fifth Wheels and Travel Trailers for Gas Leak Risk

    Highland Ridge RV is recalling 2017 Open Range, Mesa Ridge, and Roamer models because the outside range can be stored with the gas valve open, creating a fire or explosion hazard.

    Product
    HIGHLAND RIDGE FW — HIGHLAND RIDGE FW, HIGHLAND RIDGE TT OPEN RANGE, ROAMER, MESA RIDGE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·005-2017·2017-01-14

    Olymel Recalls Pork Rib Tips Produced Without Federal Inspection

    Olymel S.E.C./L.P. is recalling pork rib tips shipped to Michigan restaurants because they were repacked and distributed without the benefit of federal inspection.

    Product
    Olymel S.E.C./L.P. Recalls Pork Products Produced Without Benefit of Inspection
    Category
    Food
    Distribution
    1 state
  • SevereNHTSA·17V034000·2017-01-13

    Renegade RV Recalls Motorhomes Due to Seat Belt Anchorage Defect

    REV Recreation Group is recalling specific Renegade RV motorhomes because seat belt anchorage hardware may pull out of the floor framing during a crash.

    Product
    RENEGADE RV — RENEGADE RV VIENNA, VILLAGIO, SPECIALTY SPRINTER, CORE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·004-2017·2017-01-12

    Kettle Cuisine Recalls Chicken Soup for Misbranding and Undeclared Allergens

    Kettle Cuisine is recalling 3,096 pounds of chicken soup due to misbranding and undeclared allergens. The product was sold at Whole Foods in five states.

    Product
    Kettle Cuisine Midco, LLC — Kettle Cuisine, LLC Recalls Chicken Soup Product Due to Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    5 states
  • HighCPSC·17726·2017-01-12

    BRP Recalls Side-by-Side Off-Road Vehicles Due to Roll-Away Hazard

    BRP is recalling about 780 Can-Am Defender side-by-side off-road vehicles because they can unexpectedly roll away while in park, posing an injury risk.

    Product
    Side-by-side off-road vehicles
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·17728·2017-01-12

    Nantucket Distributing Recalls Pre-Lit Christmas Trees Due to Fire Hazard

    Nantucket Distributing is recalling pre-lit artificial Christmas trees because the fuse can overheat and blow, posing a fire hazard. No injuries have been reported.

    Product
    Pre-Lit Globe Light Christmas trees
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·17068·2017-01-12

    Boosted Recalls Electric Skateboards Due to Fire Hazard

    Boosted Inc. is recalling 2nd Generation Dual+ electric skateboards because the lithium ion battery packs can overheat and smoke, posing a fire hazard.

    Product
    Electric-powered skateboards
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·17V033000·2017-01-12

    GM Recalls 2016-2017 Chevrolet Suburban HD for Incorrect Rearview Mirror

    General Motors is recalling 2016-2017 Chevrolet Suburban HD vehicles equipped with a convex right-hand outside mirror instead of a non-convex one, which may cause drivers to misjudge distance.

    Product
    CHEVROLET — CHEVROLET SUBURBAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0908-2017·2017-01-11

    House of Flavors Recalls Peanut Butter Ice Cream for Listeria Risk

    House of Flavors, Inc. is voluntarily recalling Ashby's Sterling Peanut Butter Landslide Ice Cream because a supplier recalled peanut butter cookie dough potentially contaminated with Listeria monocytogenes.

    Product
    Ashby's Sterling Peanut Butter Landslide Ice Cream, 3 gallon container, frozen
    Category
    Food
    Distribution
    12 states
  • CriticalFDA (Food)·F-1140-2017·2017-01-11

    Chapel Hill Creamery Recalls Semi-Ripened New Moon Cheese for Salmonella Risk

    Chapel Hill Creamery is recalling Semi-Ripened New Moon cheese wheels due to potential Salmonella contamination. The product was distributed in five southeastern states.

    Product
    Semi-Ripened, New Moon, Chapel Hill Creamery, Chapel Hill, NC 27516, is sold retail by the each, .25 lb wheels, and by the 5 pack of .25 lb wheels at wholesale.
    Category
    Food
    Distribution
    5 states
  • CriticalFDA (Food)·F-1166-2017·2017-01-11

    Big Red Fresh Tomatoes Recalled for Salmonella Contamination

    Big Red Tomatoes Packers is recalling 2,521 boxes of fresh tomatoes due to Salmonella contamination. The product was distributed in Kentucky, Massachusetts, Michigan, Pennsylvania, and West Virginia.

    Product
    Big Red Fresh Tomatoes, 5x6/6x6/6x7, 25 lb cardboard boxes. Distributed by Big Red Tomatoes. Kept refrigerated.
    Category
    Food
    Distribution
    5 states
  • CriticalFDA (Food)·F-1147-2017·2017-01-11

    FDA Recalls Bulk Herring in Brine Due to Listeria Risk

    Royal Seafood Baza, Inc. is recalling 405 bulk buckets of refrigerated, ready-to-eat herring in brine due to potential Listeria monocytogenes contamination.

    Product
    Refrigerated, Ready to Eat Herring in Brine with no brand name, packaged in bulk 25 lb. white plastic bucket and labeled in part, ** 204744 ** HERRING MALOSOLNAYA (20 in barrel) ** (label on the metal handle of bucket)
    Category
    Food
    Distribution
    7 states
  • CriticalFDA (Food)·F-0845-2017·2017-01-11

    Harris Teeter Kabob Kit Recalled for Listeria Contamination Risk

    Country Fresh Products is recalling Harris Teeter Kabob Kits due to potential Listeria monocytogenes contamination. Consumers should check their freezers for affected products.

    Product
    Harris Teeter, Kabob Kit 23oz
    Category
    Food
    Distribution
    12 states
  • CriticalFDA (Food)·F-0836-2017·2017-01-11

    Country Fresh Fajita Mixes Recalled for Listeria Contamination

    Country Fresh Products is recalling specific Fajita Mixes due to potential Listeria monocytogenes contamination. Consumers in 12 states should check their pantries.

    Product
    Fajita Mixes, Net Wt.6oz, 9.5oz, 9.5oz, 10oz and 12oz, in clear plastic containers (sold under the Bi-Lo, Harris Teeter, Wal-Mart and Winn Dixie brand).
    Category
    Food
    Distribution
    12 states
  • CriticalCPSC·17067·2017-01-11

    Bad Boy Off-Road Utility Vehicles Recalled Due to Missing Seat Belts

    Textron Specialized Vehicles is recalling about 1,100 Bad Boy off-road utility vehicles because they lack seat belts, posing a risk of serious injury or death.

    Product
    Bad Boy off-road utility vehicles
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1150-2017·2017-01-11

    FDA Recalls Royal Baza Herring for Potential Listeria Contamination

    Royal Seafood Baza, Inc. is recalling 200 vacuum-packed herring products due to potential Listeria monocytogenes contamination. The products were distributed across seven states.

    Product
    Refrigerated, Ready to Eat Herring in Brine sold under the ROYAL Baza label, vacuum packaged in a clear bag and labeled in part, ** ROYAL baza ** HERRING MALOSOLNAYA IN VACUUM BY PC ** UPC 204874 000269 ** 175 Lake Ave., Staten Island, NY 10303**
    Category
    Food
    Distribution
    7 states
  • CriticalFDA (Food)·F-0846-2017·2017-01-11

    Harris Teeter Stir Fry Vegetable Recalled for Listeria Risk

    Country Fresh Products is recalling Harris Teeter Stir Fry Vegetable 10oz packages due to potential Listeria monocytogenes contamination.

    Product
    Harris Teeter, Stir Fry Vegetable 10oz
    Category
    Food
    Distribution
    12 states
  • CriticalFDA (Food)·F-1138-2017·2017-01-11

    Chapel Hill Creamery Recalls Paneer for Potential Salmonella Contamination

    Chapel Hill Creamery LLC is recalling 71.0 lbs of Paneer due to potential Salmonella contamination. The product was distributed in GA, NC, SC, TN, and VA.

    Product
    Paneer, Chapel Hill, NC 27516, is sold in cut pieces at retail and in whole wheels (about 4 lbs) wholesale.
    Category
    Food
    Distribution
    5 states
  • CriticalFDA (Food)·F-1148-2017·2017-01-11

    FDA Recalls Bulk Herring in Brine for Listeria Risk

    Royal Seafood Baza, Inc. is recalling 405 bulk buckets of refrigerated, ready-to-eat herring in brine due to potential Listeria monocytogenes contamination.

    Product
    Refrigerated, Ready to Eat Herring in Brine with no brand name, packaged in bulk 25 lb. white plastic bucket and labeled in part, ** 204883 ** HERRING DUNAYSKAYA BY PC ** (label on the metal handle of bucket)
    Category
    Food
    Distribution
    7 states
  • CriticalFDA (Food)·F-1157-2017·2017-01-11

    FDA Recalls Fresh Seafood Herring in Brine for Listeria Risk

    Royal Seafood Baza, Inc. is recalling refrigerated herring in brine due to potential Listeria monocytogenes contamination.

    Product
    Refrigerated, Ready to Eat Herring in Brine sold under the FRESH SEAFOOD label, packaged in a plastic retail container (tub), Net Wt. 46 oz. (1275g) - UPC 825512 008173 --- Produced By: R.S.B New York, NY 11691
    Category
    Food
    Distribution
    7 states
  • CriticalFDA (Food)·F-1142-2017·2017-01-11

    Chapel Hill Creamery Recalls Fresh Mozzarella Due to Salmonella Risk

    Chapel Hill Creamery is recalling Fresh Mozzarella products due to potential Salmonella contamination. The products were distributed in Georgia, North Carolina, South Carolina, Tennessee, and Virginia.

    Product
    Fresh Mozerella, Chapel Hill Creamery, Chapel Hill, NC 27516.
    Category
    Food
    Distribution
    5 states
  • CriticalFDA (Food)·F-1144-2017·2017-01-11

    FDA Recalls Bulk Herring in Brine for Listeria Risk

    Royal Seafood Baza, Inc. is recalling 405 bulk buckets of ready-to-eat herring in brine due to potential Listeria monocytogenes contamination.

    Product
    Refrigerated, Ready to Eat Herring in Brine with no brand name, packaged in bulk 25 lb. white plastic bucket and labeled in part, ** 204250 ** HERRING ISLANDSKAYA JUMBO BY PC ** (label on the metal handle of bucket)
    Category
    Food
    Distribution
    7 states
  • CriticalFDA (Food)·F-1130-2017·2017-01-11

    Chapel Hill Creamery Recalls Carolina Moon Cheese for Salmonella Risk

    Chapel Hill Creamery is recalling Carolina Moon cheese wheels due to potential Salmonella contamination. The product was distributed in five southeastern states.

    Product
    Carolina Moon, typical wheel is about .55 lb, Chapel Hill Creamery, Chapel Hill, NC 27516, sold by weight.
    Category
    Food
    Distribution
    5 states

Looking for a different month? Back to 2017.