The Recall Desk

Archive

February 2019 recalls

610 recalls were announced in February 2019.

What the numbers show

Critical
67
Severe
179
High
200
Moderate
148
Low
16

Of the 610 recalls this month scored against our rubric, 11% are Critical, 29% are Severe.

1–100 of 610

  • SevereNHTSA·19V146000·2019-02-28

    A-1 Auto Electric Recalls 2015 Freightliner CNG Vehicles for Valve Defect

    A-1 Auto Electric is recalling 2015 Freightliner 1085D and M2 refuse vehicles modified for CNG. A valve snap ring may fail if overtightened, risking injury or fire.

    Product
    FREIGHTLINER — FREIGHTLINER 1085D, M2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V143000·2019-02-28

    Chrysler Recalls 2018 Pacifica Models Due to Control Arm Separation Risk

    Chrysler is recalling 47,771 2018 Pacifica and Pacifica Plug-In Hybrid vehicles because the right front lower control arm may separate, increasing crash risk.

    Product
    CHRYSLER — CHRYSLER PACIFICA PLUG-IN HYBRID, PACIFICA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V141000·2019-02-28

    McLaren Recalls Vehicles Due to Passenger Air Bag Inflator Explosion Risk

    McLaren is recalling specific 2012-2017 models because passenger air bag inflators may explode due to propellant degradation, posing a risk of serious injury or death.

    Product
    MCLAREN — MCLAREN MP4-12C SPIDER, 675 LONGTAIL, P1, 570
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V149000·2019-02-28

    Subaru Recalls Vehicles for Brake Light Switch Malfunction Risk

    Subaru is recalling specific Impreza, WRX, Forester, and Crosstrek models because a faulty brake light switch may prevent lights from working or the vehicle from starting.

    Product
    SUBARU — SUBARU IMPREZA, WRX, FORESTER, CROSSTREK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V145000·2019-02-28

    Diamond Coach Recalls 2018 Transit Buses Due to Seat Lock Failure

    Diamond Coach is recalling 2018 Transit MPV/VTUM and PT 2000 buses because foldaway seats may not stay locked during a crash, increasing injury risk.

    Product
    DIAMOND COACH — DIAMOND COACH, DIAMOND COACH TRANSIT PT 2000, MPV/VTUM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V144000·2019-02-28

    Four Guys Recalls 2017-2018 Fire Apparatus Due to Brake Light Defect

    Four Guys is recalling 2017-2018 fire apparatus equipped with specific Whelen brake lights that may illuminate without the brake pedal being pressed.

    Product
    4 GUYS — 4 GUYS COMMERCIAL TANKER, COMMERCIAL PUMPER, CUSTOM RESCUE, CUSTOM PUMPER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·19076·2019-02-28

    Topical Anesthetic Cream Recalled for Non-Child-Resistant Packaging

    Clinical Resolution Laboratory is recalling Numb 100 Topical Anesthetic Cream because the packaging fails to meet child-resistant closure requirements, posing a poisoning risk.

    Product
    Numb 100 Topical Anesthetic Cream
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·19V147000·2019-02-28

    Triple E Recalls 2019 Serenity Motorhomes Due to Electrical Wiring Error

    Triple E is recalling 2019 Serenity S24CB motorhomes because a wiring error may prevent 120V outlets from being properly ground-fault protected, increasing the risk of electrical injury.

    Product
    TRIPLE E — TRIPLE E SERENITY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0944-2019·2019-02-27

    Satur Farms Mesclun Salad Recalled Due to Salmonella Contamination Risk

    Satur Farms LLC is recalling Mesclun Salad products due to potential Salmonella contamination. The recall affects retail and food service products distributed to New York, Florida, Connecticut, and New Jersey.

    Product
    SATUR FARMS MESCLUN SALAD Retail product is packaged in clamshell containers with Satur Farms Brand Name: 5 oz, 10 oz, 16 oz Food service product is packed in sealed poly bags: 2-1/2 lbs, 3#, 4#, 4 x 2.5#, 4 x 3#
    Category
    Food
    Distribution
    4 states
  • CriticalFDA (Food)·F-0943-2019·2019-02-27

    Satur Farms Baby Spinach Recalled for Potential Salmonella Contamination

    Satur Farms LLC is recalling baby spinach due to potential Salmonella contamination. The product was distributed to New York, Florida, Connecticut, and New Jersey.

    Product
    SATUR FARMS BABY SPINACH Retail product is packed in plastic clamshell containers with Satur Farms brand name: 5 oz, 10 oz, 16 oz Food service product is packed in sealed poly bags: 2-1/2 lbs, 3#, 4#, 4 x 2.5#, 4 x 3#
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Drugs)·D-0504-2019·2019-02-27

    Torrent Pharma Recalls Losartan Potassium and Hydrochlorothiazide Tablets Due to Impurity

    Torrent Pharma Inc. is recalling Losartan Potassium and Hydrochlorothiazide tablets because FDA labs found the impurity N-nitrosodimethylamine (NDEA) above acceptable levels.

    Product
    LOSARTAN POTASSIUM and HYDROCHLOROTHIAZIDE TABLETS, USP, 100 mg/12.5 mg, a) 90-count bottle (NDC: 13668-117-90), b) 1000-count bottle (NDC: 13668-117-10), Rx only, Manufactured by: Torrent Pharmaceuticals LTD, Indrad-382 721, Dist. Mehsana Inda
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0854-2019·2019-02-27

    Philips PageWriter TC50 ECG Devices Recalled for Overheating and Fire Risk

    Philips is recalling PageWriter TC50 electrocardiogram devices because end-of-life batteries may overheat, melt the case, or ignite, posing a risk of injury to patients and users.

    Product
    PageWriter TC50, Product 860310, Software revisions up to and including A.07.05.22 used to evaluate the electrocardiogram of adult and pediatric patients
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1014-2019·2019-02-27

    Sysco Recalls Fresh Pomegranates Due to Temperature Control Failure

    Sysco Charlotte is recalling fresh pomegranates because a cooler malfunction meant the fruit was not held at appropriate temperatures, potentially making it unsafe.

    Product
    PACKER POMEGRANATE FRESH¿
    Category
    Food
    Distribution
    3 states
  • SevereNHTSA·19V135000·2019-02-27

    BMW Recalls 2019 X7 Models Due to Loose Seat Adapter Bolts

    BMW is recalling 2019 X7 vehicles with the business lounge seat option because seat adapter bolts may not be properly tightened, increasing injury risk in a crash.

    Product
    BMW — BMW X7
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0508-2019·2019-02-27

    US Compounding Recalls Ephedrine Sulfate Syringes Due to Sterility Concerns

    US Compounding Inc is recalling 1,686 syringes of Ephedrine Sulfate 50 mg/10 mL because the company cannot ensure the product is sterile.

    Product
    Ephedrine Sulfate, 50 mg/10 mL, 10 mL Single Use Syringe, Rx only, US Compounding Pharmacy 1270 Don's Lane Conway, AR 800-718-3588, Barcode: 62295308407
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0860-2019·2019-02-27

    Philips PageWriter TC50 Recall for Battery Overheating and Ignition Risk

    Philips is recalling PageWriter TC50 devices because end-of-life batteries may overheat, melt, or ignite, posing injury risks to patients and users.

    Product
    PageWriter TC50 Government Bundle, Product 860429, Software revisions up to and including A.07.05.22 to evaluate the electrocardiogram of adult and pediatric patients
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0861-2019·2019-02-27

    Philips PageWriter TC30 Cardiograph Recall for Battery Overheating Risk

    Philips is recalling PageWriter TC30 cardiographs because end-of-life batteries may overheat, melt, or ignite, posing injury risks to patients and users.

    Product
    PageWriter TC30 w/o trolley Government Bundle, Product 860355, Software revisions up to and including A.07.05.22 to evaluate the electrocardiogram of adult and pediatric patients
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0503-2019·2019-02-27

    Torrent Pharma Recalls Losartan Potassium Tablets Due to NDEA Impurity

    Torrent Pharma Inc. is recalling Losartan Potassium Tablets because FDA testing found the impurity NDEA above acceptable levels.

    Product
    LOSARTAN POTASSIUM TABLETS, USP, 25 mg, 90-count bottle (NDC: 13668-113-90), Rx only, Manufactured by: Torrent Pharmaceuticals LTD, Indrad-382 721, Dist. Mehsana Inda
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0960-2019·2019-02-27

    Sysco Recalls Block and Barrel Cheddar Cheese Due to Temperature Issues

    Sysco Charlotte is recalling Block and Barrel Imperial Cheddar cheese because a cooler malfunction may have compromised food safety.

    Product
    Block and Barrel Imperial CHEESE CHEDDAR X SHARP LOAF YW 2/5 LB cases
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Devices)·Z-0853-2019·2019-02-27

    Philips PageWriter TC70 Cardiograph Recall for Battery Overheating Risk

    Philips is recalling PageWriter TC70 cardiographs because end-of-life batteries may overheat, melt the case, or ignite, posing a risk of injury to patients and users.

    Product
    PageWriter TC70, Product 860315, Software revisions up to and including A.07.05.22 used to evaluate the electrocardiogram of adult and pediatric patients
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0505-2019·2019-02-27

    Torrent Pharma Recalls Losartan Potassium and Hydrochlorothiazide Tablets Due to Impurity

    Torrent Pharma Inc. is recalling Losartan Potassium and Hydrochlorothiazide tablets because FDA testing found the impurity N-nitrosodimethylamine (NDEA) above acceptable levels.

    Product
    LOSARTAN POTASSIUM and HYDROCHLOROTHIAZIDE TABLETS, USP 50 mg/12.5 mg, a) 90-count bottle (NDC: 13668-116-90), b) 1000-count bottle (NDC: 13668-116-10), Rx only, Manufactured by: Torrent Pharmaceuticals LTD, Indrad-382 721, Dist. Mehsana Inda
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0501-2019·2019-02-27

    Torrent Pharma Recalls Losartan Potassium Tablets Due to NDEA Impurity

    Torrent Pharma Inc. is recalling Losartan Potassium Tablets, USP, 100 mg, because FDA testing found the impurity N-nitrosodimethylamine (NDEA) above the interim acceptable daily intake level.

    Product
    LOSARTAN POTASSIUM TABLETS, USP, 100 mg, a) 30-count (NDC: 13668-115-30), b) 90-count (NDC: 13668-115-90), c) 1000-count (NDC: 13668-115-10) per bottle, Rx only, Manufactured by: Torrent Pharmaceuticals LTD, Indrad-382 721, Dist. Mehsana Inda
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1001-2019·2019-02-27

    Sysco Recalls Majestic Blue Crab Meat Due to Temperature Control Failure

    Sysco Charlotte is recalling Majestic Blue Crab Meat Super Lump because a cooler malfunction meant the product was not held at appropriate temperatures, potentially making it unsafe.

    Product
    Majestic Blue CRAB MEAT SUPER LUMP PAST MEX
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Devices)·Z-0856-2019·2019-02-27

    Philips PageWriter TC20 Recall for Battery Overheating and Fire Risk

    Philips is recalling PageWriter TC20 devices because end-of-life batteries may overheat, melt the case, or ignite, posing a risk of injury.

    Product
    PageWriter TC20, Product 860332, Software revisions up to and including A.07.05.22 to evaluate the electrocardiogram of adult and pediatric patients
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0850-2019·2019-02-27

    Baxter Recalls Kaguya Automated Peritoneal Dialysis Systems Due to Software Defect

    Baxter Healthcare is recalling 1,085 Kaguya Automated Peritoneal Dialysis Systems because a software defect may cause shortened dwell times during therapy.

    Product
    Kaguya Automated Peritoneal Dialysis System Product Usage: It is intended for automatic control of dialysate solution exchanges in the treatment of adult renal failure patients undergoing Peritoneal dialysis.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0502-2019·2019-02-27

    Torrent Pharma Recalls Losartan Potassium Tablets Due to NDEA Impurity

    Torrent Pharma Inc. is recalling Losartan Potassium Tablets, 50 mg, because FDA testing found the impurity N-nitrosodimethylamine (NDEA) above acceptable levels.

    Product
    LOSARTAN POTASSIUM TABLETS, USP, 50 mg, a) 30-count bottle (NDC: 13668-409-30), b) 90-count bottle (NDC: 13668-409-90), c) 1000-count bottle (NDC: 13668-409-10), Rx only, Manufactured by: Torrent Pharmaceuticals LTD, Indrad-382 721, Dist. Mehsana Inda
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0855-2019·2019-02-27

    Philips PageWriter TC30 ECG Devices Recalled for Overheating and Ignition Risk

    Philips is recalling PageWriter TC30 ECG devices because end-of-life batteries may overheat, melt the case, or ignite, posing injury risks to patients and users.

    Product
    PageWriter TC30, Product 860306, Software revisions up to and including A.07.05.22 to evaluate the electrocardiogram of adult and pediatric patients
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0859-2019·2019-02-27

    Philips PageWriter TC30 Cardiograph Recall for Battery Overheating Risk

    Philips is recalling PageWriter TC30 cardiographs because end-of-life batteries may overheat, melt, or ignite, posing injury risks to patients and users.

    Product
    PageWriter TC30 w/ trolley Government Bundle, Product 860354, Software revisions up to and including A.07.05.22 to evaluate the electrocardiogram of adult and pediatric patients
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0509-2019·2019-02-27

    ICU Medical Recalls 0.9% Sodium Chloride Injection Due to CGMP Deviations

    ICU Medical Inc. is voluntarily recalling 475,320 bags of 0.9% Sodium Chloride Injection due to Current Good Manufacturing Practice (CGMP) deviations.

    Product
    0.9% Sodium Chloride Injection, USP 1000 mL flexible container, Rx only, Hospira, Inc., Lake Forest, IL 60045 USA, NDC 0409-7983-09
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0858-2019·2019-02-27

    Philips PageWriter TC Cardiograph Recall for Battery Overheating and Fire Risk

    Philips is recalling PageWriter TC70 cardiographs because end-of-life batteries may overheat, melt, or ignite, posing injury risks to patients and users.

    Product
    PageWriter TC70 w/o trolley Government Bundle, Product 860353, Software revisions up to and including A.07.05.22 to evaluate the electrocardiogram of adult and pediatric patients
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1050-2019·2019-02-27

    Boston Smoked Fish Company Recalls Nova Lox Sides Due to Low Salt Levels

    The Boston Smoked Fish Company is recalling Nova Lox Sides because the product had low water phase salt levels. The recall affects 29.45 lbs distributed in Massachusetts.

    Product
    BOSTON SMOKED FISH CO. Nova Lox Sides, 5 packages of 2 pound units in corrugated box, Store at or below 38 deg, UPC: (01)90857016007065(3202)100000
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Devices)·Z-0857-2019·2019-02-27

    Philips PageWriter TC70 Cardiograph Recall for Battery Overheating Risk

    Philips is recalling 57 PageWriter TC70 cardiographs because end-of-life batteries may overheat, melt, or ignite, posing a risk of injury to patients and users.

    Product
    PageWriter TC70 w/trolley Government Bundle, Product 860352, Software revisions up to and including A.07.05. 22 to evaluate the electrocardiogram of adult and pediatric patients
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1048-2019·2019-02-27

    Katy's Kitchen Roasted Sunflower Kernels Recalled for E. coli Contamination

    Marathon Ventures Inc is recalling Katy's Kitchen Roasted and Salted Sunflower Kernels due to potential E. coli contamination. The product was distributed to one customer in Nebraska.

    Product
    Katy's Kitchen Roasted and Salted Sunflower Kernals, Net Wt. 25 lbs,
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-0987-2019·2019-02-27

    Sysco Recalls Harbor Seafood Crab Meat Due to Temperature Failure

    Sysco Charlotte is recalling Harbor Seafood Crab Meat Backfin Past Asia because a cooler malfunction caused the product to be held at unsafe temperatures.

    Product
    Harbor Seafood CRAB MEAT BACKFIN PAST ASIA
    Category
    Food
    Distribution
    3 states
  • HighFDA (Devices)·Z-0847-2019·2019-02-27

    bioMerieux Recalls VITEK 2 AST-N351 Test Kits Due to False Positives

    bioMerieux, Inc. is recalling VITEK 2 AST-N351 Test Kits distributed in the UK and Ireland because they may produce false positive results for ESBL phenotypes.

    Product
    VITEK 2 AST-N351 Test Kit
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0846-2019·2019-02-27

    Teleflex Recalls Pilling Cooley Sump-Suction Tubes Due to Missing Tip

    Teleflex Medical is recalling 80 units of Pilling Cooley Sump-Suction Tubes because a missing internal tip prevents the device from functioning as intended.

    Product
    Pilling COOLEY SUMP-SUCTION TUBE, REF 351547
    Category
    Medical Device
    Distribution
    3 states
  • HighFDA (Devices)·Z-0852-2019·2019-02-27

    Boston Scientific Recalls Mislabelled Stingray Guidewires for Coronary Procedures

    Boston Scientific is recalling 49 Stingray Guidewires that are 185cm but incorrectly labeled as 300cm. The mislabeling could lead to improper use during angioplasty procedures.

    Product
    Stingray" Guidewire, labeled as 300cm. intended to facilitate placement of balloon dilatation catheters or other intravascular devices during percutaneous transluminal coronary angioplasty (PTCA) and percutaneous transluminal angioplasty (PTA).
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·19E017000·2019-02-27

    Specialty Manufacturing Recalls Transpec T287X Series Glass Roof Hatches

    Specialty Manufacturing is recalling Transpec T287X Series glass roof hatches because temperature and vibration stresses may cause the tempered glass to shatter, posing an injury risk to passengers.

    Product
    STRUCTURE:EMERGENCY:ESCAPE/EGRESS/EXIT recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0990-2019·2019-02-27

    Sysco Recalls Crab Meat Claw Pstrzd Asia Due to Temperature Malfunction

    Sysco Charlotte is recalling Chicken of the Sea and Sebastian Superior crab meat because a cooler malfunction may have compromised food safety.

    Product
    CRAB MEAT CLAW PSTRZD ASIA Sold under the brand names of Chicken of the Sea & Sebastian Superior
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·F-0998-2019·2019-02-27

    Sysco Recalls Sea Wings Crab Meat Special Due to Temperature Failure

    Sysco Charlotte is recalling Sea Wings CRAB MEAT SPECIAL PAST ASIA because a cooler malfunction meant the food was not held at appropriate temperatures, potentially making it unsafe.

    Product
    Sea Wings CRAB MEAT SPECIAL PAST ASIA
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·F-0941-2019·2019-02-27

    Ardent Mills Recalls Self-Rising Flour Due to Salmonella Risk

    Ardent Mills is voluntarily recalling certain lots of Westcreek Self-Rising Flour because they may be contaminated with Salmonella.

    Product
    WESTCREEK H&R SELF RISE AP FLR 25LB and 50LB
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0864-2019·2019-02-27

    Shimadzu TRINIAS Imaging Systems Recalled for Software and Display Errors

    Shimadzu is recalling 13 TRINIAS imaging systems due to software crashes and rare display corruption that may hinder medical examinations.

    Product
    TRINIAS for diagnostic imaging and interventional procedures in cardiac angiography, neurovascular angiography, abdominal angiography, peripheral angiography, rotational angiography, multi-purpose angiography and whole body radiographic/fluoroscopic procedures.
    Category
    Medical Device
    Distribution
    9 states
  • HighFDA (Food)·F-1049-2019·2019-02-27

    Barley Lentil Dry Soup Base Recalled for Undeclared Wheat and Soy

    The Secret Garden of Park Rapids is recalling Barley Lentil Dry Soup Base packages because they may contain undeclared wheat and soy.

    Product
    Barley Lentil Dry soup base. UPC 91675-06002. the Secret Garden, Park Rapids, MN 56470
    Category
    Food
    Distribution
    1 state
  • HighNHTSA·19V140000·2019-02-27

    Midway Recalls One 2016 Freightliner Sprinter 3500 Wheelchair Lift Vehicle

    Midway Specialty Vehicles is recalling one 2016 Freightliner Sprinter 3500 because a wheelchair lift component may fail, causing the platform to rise too high and increasing injury risk.

    Product
    FREIGHTLINER — FREIGHTLINER SPRINTER 3500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1017-2019·2019-02-27

    Sysco Recalls Fresh Chopped Salad Due to Temperature Malfunction

    Sysco Charlotte is recalling TAYFRMS SALAD FRESH CHPD WORLD FAMOUS because a cooler malfunction may have allowed the product to be held at unsafe temperatures.

    Product
    TAYFRMS SALAD FRESH CHPD WORLD FAMOUS¿
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·F-0942-2019·2019-02-27

    Ardent Mills Recalls Self-Rising Flour Due to Salmonella Risk

    Ardent Mills is voluntarily recalling specific lots of Members Mark Self-Rising Flour because they may be contaminated with Salmonella.

    Product
    MEMBERS MARK SELF RISE FLR 25LB
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0939-2019·2019-02-27

    Ardent Mills Recalls Self-Rising Flour Lots for Potential Salmonella Contamination

    Ardent Mills is voluntarily recalling specific lots of self-rising flour due to potential Salmonella contamination. The affected products were distributed nationwide.

    Product
    ARDENT H&R SR FLR, 25LB, 50 LB, and 25LB (PC)-309951, packaged in paper bags, Store at Ambient Temperature
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·19V134000·2019-02-27

    Lexus Recalls 2018 LS Models for Run-Flat Tire Defect

    Toyota is recalling 2018 Lexus LS vehicles because run-flat tires may have cracked reinforcement layers, potentially causing tread separation and affecting vehicle stability.

    Product
    LEXUS — LEXUS LS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0507-2019·2019-02-27

    Dr. Reddy's Recalls Divalproex Sodium Tablets for Dissolution Failure

    Dr. Reddy's is recalling 10,656 bottles of Divalproex Sodium Extended-release Tablets because they failed to meet dissolution specifications.

    Product
    DIVALPROEX SODIUM — DIVALPROEX SODIUM (DIVALPROEX SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0849-2019·2019-02-27

    Baxter AMIA Automated Peritoneal Dialysis System Software Recall

    Baxter is recalling 7,688 AMIA Automated Peritoneal Dialysis Systems due to a software defect that may cause shortened dwell times during therapy.

    Product
    AMIA Automated Peritoneal Dialysis System Product Usage: It is intended for automatic control of dialysate solution exchanges in the treatment of adult renal failure patients undergoing Peritoneal dialysis.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0848-2019·2019-02-27

    Ortho-Clinical Diagnostics Recalls VITROS VALP Reagent Packs Due to Negative Bias

    Ortho-Clinical Diagnostics is recalling VITROS Chemistry Products VALP Reagent Packs because they may produce negative bias results when measuring valproic acid.

    Product
    VITROS Chemistry Products VALP Reagent Pack. For in vitro diagnostic use only. CATALOG #(s): 6801710 INTENDED USE: For in vitro diagnostic use only. VITROS Chemistry Products VALP Reagent is used on the VITROS 5,1 FS Chemistry System, the VITROS 4600 Chemistry System and
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0992-2019·2019-02-27

    Sysco Recalls Van Camp Crab Meat Due to Temperature Malfunction

    Sysco Charlotte is recalling Van Camp Crab Meat because a cooler malfunction may have allowed the product to be held at unsafe temperatures.

    Product
    Van Camp CRAB MEAT HAANII LUMP PAST
    Category
    Food
    Distribution
    3 states
  • HighCPSC·19074·2019-02-27

    Harbor Freight Recalls Greenwood Propane Torches Due to Burn Hazard

    Harbor Freight Tools is recalling Greenwood propane torches because the trigger can fail to disengage, posing a burn hazard. One burn injury has been reported.

    Product
    Greenwood propane torches
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·19V137000·2019-02-27

    Freightliner Recalls 2020 Cascadia Trucks for Incorrect Gear Display

    Daimler Trucks is recalling 2020 Freightliner Cascadia trucks because the instrument cluster may incorrectly display 'Neutral' when the truck is in gear, increasing crash risk.

    Product
    FREIGHTLINER — FREIGHTLINER CASCADIA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V133000·2019-02-27

    Triumph Recalls Motorcycles Due to Clutch Cable Wiring Damage Risk

    Triumph is recalling specific 2016-2019 motorcycles because the clutch cable may damage wiring, potentially causing electrical failures or engine stalling.

    Product
    TRIUMPH — TRIUMPH SCRAMBLER, STREET TWIN, BONNEVILLE T120 BLACK, STREET CUP
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0938-2019·2019-02-27

    Century Snacks Recalls Praline Pecans Due to Mispackaging

    Century Snacks LLC is recalling 25 packages of Praline Pecans because they were mispackaged with Praline Almonds. The error creates an undeclared allergen risk for consumers with nut allergies.

    Product
    Snak Club Praline Pecans Made With Cane Sugar NET Wt. 2.25 oz (64 g) Produced By: Century Snack Commerce, CA 90040 centurysnacks.com
    Category
    Food
    Distribution
    6 states
  • HighFDA (Food)·F-1000-2019·2019-02-27

    Sysco Recalls Harbor Seafood Crab Meat Due to Temperature Malfunction

    Sysco Charlotte is recalling Harbor Seafood Crab Meat Super Lump because a cooler malfunction may have allowed the product to be held at unsafe temperatures.

    Product
    Harbor Seafood CRAB MEAT SUPER LUMP PAST ASIA
    Category
    Food
    Distribution
    3 states
  • HighFDA (Devices)·Z-0845-2019·2019-02-27

    Medtronic Power Supply and Programmer Recall for Electrical Short Risk

    Medtronic is recalling 731 Power Supply 26907 and CareLink Encore 29901 Programmer units due to a potential electrical short circuit that can cause heating and smoke.

    Product
    Medtronic Power Supply 26907, Medtronic CareLink Encore(TM) 29901 Programmer
    Category
    Medical Device
    Distribution
    1 state
  • ModerateFDA (Food)·F-0964-2019·2019-02-27

    Sysco Recalls Cheese Cubes Due to Cooler Malfunction and Temperature Issues

    Sysco Charlotte is recalling Block and Barrel Imperial cheese cubes because a cooler malfunction prevented proper temperature holding, potentially making the food unsafe.

    Product
    Block and Barrel Imperial CHEESE CUBE CHED/SWISS/PEP JCK 3/5 lb blocks
    Category
    Food
    Distribution
    3 states
  • ModerateFDA (Food)·F-0953-2019·2019-02-27

    Sysco Recalls Roth Kase Cheese Blend Due to Temperature Control Failure

    Sysco Charlotte is recalling Roth Kase Cheese Blend because a cooler malfunction prevented the food from being held at appropriate temperatures, potentially making it unsafe.

    Product
    Roth Kase CHEESE BLND FIREHOUSE ULTMTE 2/5lb CASE
    Category
    Food
    Distribution
    3 states
  • ModerateFDA (Drugs)·D-0496-2019·2019-02-27

    Advanced Pharma Recalls Fentanyl Syringes Due to Incorrect Expiration Date

    Advanced Pharma Inc. is recalling 100 syringes of Fentanyl in 0.9% Sodium Chloride due to an incorrect expiration date on the label.

    Product
    Fentanyl in 0.9% Sodium Chloride QS 0.5 mL, 5 mcg/0.5 mL with up to 0.1 mL of overfill Injectable Solution, Sterile single use syringe, Rx only, Avella of Houston 9265 Kirby Dr., Houston, TX 77054 (877) 794-0404, NDC 42852-210-72
    Category
    Drug
    Distribution
    1 state
  • ModerateFDA (Food)·F-1047-2019·2019-02-27

    Nutrafuels Recalls CTFO Weight Loss Oral Spray Due to Microbial Contamination

    Nutrafuels, Inc. is recalling CTFO Weight Loss Oral Spray because third-party testing found Enterobacteriaceae contamination in specific lots.

    Product
    CTFO Weight Loss Oral Spray with pure CBD Hemp Oil isolate Dietary Supplement, 1oz/30ml.
    Category
    Food
    Distribution
    0 states

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