The Recall Desk

Archive

June 2022 recalls

857 recalls were announced in June 2022.

What the numbers show

Critical
29
Severe
235
High
450
Moderate
141
Low
2

Of the 857 recalls this month scored against our rubric, 3% are Critical, 27% are Severe.

501–600 of 857

  • ModerateFDA (Food)·F-1272-2022·2022-06-15

    Zydot Detox Drink Recalled for Missing Ingredient Declarations

    Zydot Unlimited recalls 1,150 bottles of Zydot Ultimate Blend detox drink due to undeclared preservatives and food colorants on the label.

    Product
    Zydot Ultimate Blend The Original Detox Drink Natural Tropical Ice Flavor 16 fl. oz. (473 ml) UPC packaged in plastic bottle with lid
    Category
    Food
    Distribution
    0 states
  • ModerateFDA (Drugs)·D-1090-2022·2022-06-15

    Proventil HFA albuterol inhalers recalled for manufacturing temperature deviation

    Proventil HFA inhalers are being recalled nationwide by McKesson Medical-Surgical due to temperature abuse during manufacturing, a deviation from FDA Good Manufacturing Practice standards.

    Product
    Proventil HFA, (Albuterol Sulfate Inhalation Aerosol), 200 metered inhalations, Rx only, MFG: Merck Company, NDC 0085-1132-04
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1106-2022·2022-06-15

    Triamcinolone Acetonide Cream Recalled Due to Temperature Abuse During Manufacturing

    McKesson Medical-Surgical is recalling Triamcinolone Acetonide cream nationwide due to cGMP deviations related to temperature abuse during manufacturing. Specific lot numbers of affected product could not be identified.

    Product
    TRIAMCINOLONE ACETONIDE — TRIAMCINOLONE ACETONIDE (TRIAMCINOLONE ACETONIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1069-2022·2022-06-15

    Medroxyprogesterone acetate injection recalled due to temperature abuse manufacturing deviation

    McKesson Medical-Surgical is recalling medroxyprogesterone acetate injectable suspension (150 mg/mL) due to temperature abuse during manufacturing. The affected vials were distributed nationwide; patients should contact their healthcare provider.

    Product
    Medroxyprogesterone acetate injectable suspension, USP, 150 mg/mL, 1 mL vials, packaged in a) single dose vial (NDC 0703-6801-01), b) 25-count box single dose vials (NDC 0703-6801-04), Rx only, MFG: Teva Pharma USA
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1081-2022·2022-06-15

    Prescription injection Revonto recalled due to manufacturing temperature deviation

    Revonto (dantrolene sodium) injection is being recalled due to manufacturing deviations involving temperature abuse. Approximately 49 cartons were distributed nationwide; healthcare providers should contact their supplier for guidance.

    Product
    REVONTO — REVONTO (DANTROLENE SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1107-2022·2022-06-15

    Polymyxin B and Trimethoprim Ophthalmic Solution Recalled Due to Temperature Abuse

    McKesson Medical-Surgical is recalling Polymyxin B and Trimethoprim Ophthalmic Solution nationwide due to temperature deviations during manufacturing. The medication may not work as intended.

    Product
    Polymyxin B Sulfate and Trimethoprim Ophthalmic Solution, USP, sterile, 0.1%, 10 mL bottle, Rx only, MFG: Sandoz Pharma, NDC 6131462810
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1028-2022·2022-06-15

    FDA Recalls Betamethasone Dipropionate Cream for Temperature-Abuse Storage Deviations

    McKesson Medical-Surgical is recalling Betamethasone Dipropionate Cream USP 0.05% due to temperature-abuse cGMP deviations. The FDA Class II recall affects nationwide distribution.

    Product
    Betamethasone Dipropionate Cream USP, 0.05%, 45 grams tube, Rx only, MFG: Sandoz Pharma, NDC 0168-0055-46
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0999-2022·2022-06-15

    Bupivacaine Injectable Recalled for Temperature Abuse During Manufacturing

    McKesson Medical-Surgical is recalling Bupivacaine HCl Injection vials (NDC 55150-0170-30) distributed nationwide due to temperature abuse during manufacturing that may affect product quality. No illnesses have been reported.

    Product
    Bupivacaine HCl Injection, single dose vial, 0.5%, 30 mL/5 mg/mL, Rx only, Manufacturer: Auromedics Pharma LLC, NDC 55150-0170-30
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1113-2022·2022-06-15

    Tetracaine Hydrochloride Ophthalmic Solution Recalled for Temperature Abuse

    McKesson Medical-Surgical is recalling Tetracaine Hydrochloride Ophthalmic Solution due to cGMP deviations from temperature abuse. The recall affects 43 cartons distributed nationwide.

    Product
    TETRACAINE HYDROCHLORIDE — TETRACAINE HYDROCHLORIDE (TETRACAINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1032-2022·2022-06-15

    Doxycycline Capsules Recalled for Temperature Control Deviation

    McKesson Medical-Surgical is recalling Doxycycline Capsules, USP, 100 mg due to temperature abuse during manufacturing. The Class II recall affects 3 bottles distributed nationwide across the USA.

    Product
    DOXYCYCLINE — DOXYCYCLINE (DOXYCYCLINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1049-2022·2022-06-15

    Nitrostat Nitroglycerin Tablets Recalled Due to Temperature Abuse During Manufacturing

    McKesson Medical-Surgical is recalling Nitrostat (nitroglycerin sublingual tablets) 0.4 mg due to manufacturing deviations involving temperature abuse that may affect product quality. The affected product was distributed nationwide.

    Product
    Nitrostat (Nitroglycerin Sublingual Tablets, USP) 0.4 mg/tablet, 25-count bottle, Rx only, Distributed by: Pfizer Parke-Davis, Division of Pfizer Inc., NDC 0071-0418-13
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1011-2022·2022-06-15

    FDA Recalls Dihydroergotamine Mesylate Injection for Temperature Abuse

    McKesson Medical-Surgical is recalling Dihydroergotamine Mesylate Injection (NDC 0574-0850-10) due to temperature deviations during manufacturing that may affect product quality. The drug was distributed nationwide.

    Product
    Dihydroergotamine Mesylate, Injection, USP, 1mg/mL, packaged in box of 5 x 1 mL ampules, Rx only, Manufactured for: Perrigo, Minneapolis, MN, NDC 0574-0850-10
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1006-2022·2022-06-15

    Arzol Silver Nitrate Applicator Recalled for Temperature-Related Manufacturing Defects

    McKesson Medical-Surgical is recalling Arzol silver nitrate applicators nationwide due to temperature abuse during manufacturing that may affect product quality.

    Product
    Arzol (Silver Nitrate Applicator), (Silver Nitrate 75%, Potassium Nitrate 25%), 100-count box, Rx only, Manufacturer: Arzol Chemical Co, NDC 12870-0001-02
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1036-2022·2022-06-15

    FDA Recalls MIOSTAT Carbachol Solution Nationwide for Temperature Abuse

    McKesson Medical-Surgical is recalling MIOSTAT (Carbachol Intraocular Solution) nationwide due to temperature abuse during distribution that may affect medication stability.

    Product
    MIOSTAT — MIOSTAT (CARBACHOL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1047-2022·2022-06-15

    FDA recalls Lidocaine-Prilocaine topical anesthetic cream for temperature abuse

    McKesson Medical-Surgical is recalling Lidocaine and Prilocaine Cream due to cGMP deviations involving temperature abuse during distribution. The recall affects 23 tubes distributed nationwide.

    Product
    LIDOCAINE AND PRILOCAINE — LIDOCAINE AND PRILOCAINE (LIDOCAINE AND PRILOCAINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·22V421000·2022-06-14

    Kaufman Recalls 2018-2021 Trailers Due to Insufficient Ramp Bracket Welds

    Kaufman is recalling 2018-2021 FXSG-10K-20D and FXSG-10K-20D-SC trailers because insufficient welds on the ramp holding bracket may allow the ramp to fall, increasing injury risk.

    Product
    KAUFMAN — KAUFMAN FXSG-10K-20D-SC, FXSG-10K-20D
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V418000·2022-06-13

    Thomas Built Buses Recalls 2021-2023 Saf-T-Liner C2 Jouley Electric Buses

    Daimler Trucks North America is recalling 2021-2023 Thomas Built Buses Saf-T-Liner C2 Jouley electric buses due to a high voltage battery cable defect that may cause power loss, ground short circuits, or fire.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER C2 JOULEY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·019-2022·2022-06-13

    Yumei Foods Recalls Ineligible Imported Siluriformes Fish Products

    Yumei Foods USA, Inc. is recalling approximately 9,370 pounds of imported fish products because China is ineligible to export processed Siluriformes to the U.S.

    Product
    Yumei Foods USA, Inc. Recalls Ineligible Siluriformes Products Imported from China
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V420000·2022-06-13

    Nissan Recalls 2013-2016 Pathfinders for Hood Latch Malfunction

    Nissan is recalling 2013-2016 Pathfinders because the secondary hood latch may fail to secure, potentially allowing the hood to open while driving and obstructing the driver's view.

    Product
    NISSAN — NISSAN PATHFINDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V416000·2022-06-13

    Nova Bus Recalls LFS Models Due to Electrical Fire Risk

    Nova Bus is recalling 2019-2022 LFS and LFS Artic buses because a corroded fuse holder may cause an electrical short, increasing the risk of a fire.

    Product
    NOVA BUS — NOVA BUS LFS ARTIC, LFS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V417000·2022-06-13

    Utilimaster Walk-In Van Recall for Incorrectly Installed Passenger Headrest

    Shyft Group is recalling 2021-2022 Utilimaster Walk-In Vans because the passenger-side jump seat headrest may be installed incorrectly, increasing injury risk in a crash.

    Product
    UTILIMASTER — UTILIMASTER WALK-IN VAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V419000·2022-06-13

    Kentucky Trailer MV and PV Recall for Loose Walk Board Rack Bolts

    Kentucky Trailer Manufacturing is recalling 2014-2021 MV and PV trailers because walk board rack bolts may loosen, allowing the rack to separate and fall.

    Product
    KENTUCKY TRAILER — KENTUCKY TRAILER MV, PV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V414000·2022-06-10

    Ford Recalls One 2021 F-150 for Unsecured Fuel Tank Strap

    Ford is recalling one 2021 F-150 because the fuel tank front attachment may be missing, increasing the risk of a fuel leak and fire.

    Product
    FORD — FORD F-150
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V411000·2022-06-10

    Ford Bronco passenger-side door child safety lock malfunction

    Ford is recalling 2021-2022 Bronco four-door vehicles because the passenger-side rear door can open from inside the vehicle when the child safety lock is in the "ON" position, increasing the risk of injury to child occupants.

    Product
    FORD — FORD BRONCO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V413000·2022-06-10

    Ford Transit Connect Shifter Cable Bushing May Cause Gear Shift Failures

    Ford is recalling 2013-2021 Transit Connect vehicles because the shifter cable bushing may degrade and prevent intended gear selection. This can cause unintended vehicle movement or rollaway after selecting Park, increasing crash and injury risk.

    Product
    FORD — FORD FUSION, EDGE, C-MAX, TRANSIT CONNECT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V406000·2022-06-09

    Chrysler Recalls 2014-2020 Jeep and Ram 1500 Diesel Vehicles

    Chrysler is recalling 2014-2020 Jeep Grand Cherokee and 2014-2019 Ram 1500 diesel vehicles because a fuel pump failure may cause fuel starvation and loss of drive power.

    Product
    RAM — RAM, JEEP 1500, GRAND CHEROKEE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V408000·2022-06-09

    Roush CleanTech Recalls Ford Trucks Due to Fuel Line Corrosion Risk

    Roush CleanTech is recalling 3,285 altered 2016-2022 Ford trucks because zinc plating on fuel return lines may break away, causing corrosion and increasing fire risk.

    Product
    ROUSH CLEANTECH — ROUSH CLEANTECH FORD F-450, FORD F-53, FORD F-650, FORD F-750
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·22155·2022-06-09

    Brompton Electric Folding Bicycles Recalled for Crash and Injury Hazards

    Brompton is recalling about 2,230 electric folding bicycles because the mudguard is positioned too close to the front wheel, which can lock up and cause the bike to crash. The company has received 10 reports of crashes resulting in nine injury reports and two hospitalizations.

    Product
    Brompton Electric Folding Bicycles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·22E049000·2022-06-09

    Roush Recalls LPG Fuel Return Lines Due to Corrosion Risk

    Roush CleanTech is recalling specific LPG fuel return lines installed on vehicles in 24 states and D.C. due to a corrosion risk that could cause fuel leaks and fire.

    Product
    FUEL SYSTEM, OTHER:DELIVERY:HOSES, LINES/PIPING, AND FITTINGS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V407000·2022-06-09

    2022 RAM Pickup Trucks Recalled for Rearview Camera Display Failure

    Certain 2022 RAM 1500, 2500, and 3500 pickup trucks may have defective radio software that prevents the rearview camera image from displaying, reducing rear visibility and increasing crash risk.

    Product
    RAM — RAM 2500, 1500, 3500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·22154·2022-06-09

    Spirit Halloween 48-Inch Black Light Fixtures Recalled for Fire and Burn Hazards

    Spirit Halloween is recalling about 12,400 units of 48-inch black light fixtures sold from August to November 2021. The bulb can pop, flash, overheat, and catch fire, posing fire and burn hazards.

    Product
    Spirit Halloween 48" Black Lights
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·018-2022·2022-06-09

    Northern Tier Bakery Recalls Ready-To-Eat Salads Due to Listeria Risk

    Northern Tier Bakery, LLC is recalling approximately 905 pounds of ready-to-eat salad products sold in Minnesota and Wisconsin due to possible Listeria monocytogenes contamination.

    Product
    Northern Tier Bakery, LLC — Northern Tier Bakery, LLC Recalls Ready-To-Eat Salad Products Due to Possible Listeria Contamination
    Category
    Food
    Distribution
    2 states
  • HighNHTSA·22V410000·2022-06-09

    Forest River Recalls 2022 Prime Time Fifth Wheel Travel Trailers

    Forest River is recalling 2022 Prime Time Crusader and Sanibel fifth wheel travel trailers because step treads may detach, increasing injury risk.

    Product
    PRIME TIME — PRIME TIME SANIBEL, CRUSADER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·22152·2022-06-09

    Intimidator and Mahindra Utility Vehicles Recalled for Crash Hazard

    About 16,000 Intimidator and Mahindra utility vehicles (UTVs) are being recalled because the throttle cable can freeze in cold temperatures, causing a stuck throttle and brake failure. Additionally, certain Model Year 2022 Intimidator GC1K vehicles lack speed-limiting software when the seatbelt is disengaged.

    Product
    Intimidator and Mahindra branded utility vehicles (UTVs)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22E048000·2022-06-09

    Chrysler Recalls Mopar Diesel Fuel Pumps for Potential Fuel Starvation

    Chrysler is recalling specific Mopar high-pressure fuel pumps and 3.0L diesel engines because pump failure may cause fuel starvation and loss of drive power.

    Product
    FUEL SYSTEM, DIESEL:DELIVERY:FUEL PUMP recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·22151·2022-06-09

    Hisense French Door Refrigerators Recalled for Door Detachment Injury Risk

    Hisense USA is recalling about 55,200 French door refrigerators because the door hinge can break and cause the door to detach, posing an impact injury hazard. The firm has received reports of five injuries including foot bruises and lacerations.

    Product
    Hisense French Door Refrigerators with Ice Maker
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·22750·2022-06-09

    Jungle Jumparoo Children's Toys Recalled for Excess Lead in Poles

    Jungle Jumparoo children's toys sold online from November 2018 through March 2019 contain yellow poles with lead levels exceeding the federal ban. Lead is toxic if ingested and can cause adverse health effects in young children.

    Product
    Jungle Jumparoo Children's Toys
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateCPSC·22153·2022-06-09

    Nautilus Treadmills Recalled Due to Fall Hazard Risk

    Nautilus is recalling about 7,300 treadmills because they can start on their own, creating a fall hazard. No injuries have been reported to date.

    Product
    Nautilus Treadmills
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateCPSC·22156·2022-06-09

    Manhattan Toy Company Recalls Activity Loops Toys for Choking Hazard

    The Manhattan Toy Company is recalling its Activity Loops toys because tubes can detach from the base and release small plastic rings that pose a choking hazard to children. No injuries have been reported.

    Product
    Activity Loops
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1125-2022·2022-06-08

    Jif Peanut Butter Recalled for Potential Salmonella Contamination

    The FDA recalled JIF 16 Ounce Creamy Omega 3 Peanut Butter due to potential Salmonella contamination. Approximately 33,516 cases distributed nationwide are affected.

    Product
    JIF 16 OUNCE CREAMY OMEGA 3 PEANUT BUTTER
    Category
    Food
    Distribution
    49 states
  • CriticalFDA (Food)·F-1134-2022·2022-06-08

    Mary's Harvest Apple Peanut Butter Cups recalled for Salmonella contamination

    Mary's Harvest brand Apple Peanut Butter Cups are being recalled due to potential Salmonella contamination. The recall affects 450 cups distributed in Oregon and Washington with use-by dates between May 15 and May 30, 2022.

    Product
    Mary's Harvest brand, Apple Peanut Butter Cup G&G, net wt. per cup 6.5 oz., UPC8 87241 79671 4.
    Category
    Food
    Distribution
    2 states
  • CriticalFDA (Food)·F-1112-2022·2022-06-08

    JIF Natural Peanut Butter Recalled for Potential Salmonella Contamination

    JIF Natural Peanut Butter in 0.64 oz individual packs is being recalled due to potential Salmonella contamination. The recall affects 47,918 cases distributed nationwide.

    Product
    JIF NATURAL PEANUT BUTTER packaged in 0.64oz and 96 count
    Category
    Food
    Distribution
    49 states
  • CriticalFDA (Food)·F-1147-2022·2022-06-08

    Assorted Chocolate Heart Boxes Recalled for Potential Salmonella Contamination

    Walnut Creek Chocolate Co Inc is recalling Assorted Chocolate Heart Boxes due to potential Salmonella contamination. Consumers should not consume the recalled products.

    Product
    Assorted Chocolate Heart Boxes packaged in 8oz and 16oz boxes
    Category
    Food
    Distribution
    29 states
  • CriticalFDA (Food)·F-1118-2022·2022-06-08

    JIF Reduced Fat Peanut Butter Recalled for Potential Salmonella Contamination

    The JM Smucker Company is recalling JIF Reduced Fat Creamy Peanut Butter in 16-ounce and 40-ounce containers due to potential Salmonella contamination. The recall affects approximately 454,971 cases distributed nationwide.

    Product
    JIF REDUCED FAT CREAMY PEANUT BUTTER packaged in 16oz and 40oz
    Category
    Food
    Distribution
    49 states
  • SevereFDA (Food)·F-1137-2022·2022-06-08

    Seasonal Peanut Butter Cups recalled for potential Salmonella contamination

    Walnut Creek Chocolate Co Inc is recalling Seasonal Peanut Butter Cup Gift Boxes due to potential Salmonella contamination. The 4oz boxes with Lot Code 1362 have been distributed across multiple states.

    Product
    Seasonal Peanut Butter Cup Gift Boxes packaged in 4oz, 8 piece boxes
    Category
    Food
    Distribution
    29 states
  • SevereFDA (Food)·F-1126-2022·2022-06-08

    JIF Crunchy Peanut Butter Recall: Potential Salmonella Contamination

    The JM Smucker Company is recalling JIF Crunchy Peanut Butter (40 oz) due to potential Salmonella contamination. Affected products have lot codes 1274425 or 2140425 with best-by dates from October 1, 2023 to May 20, 2024.

    Product
    JIF 40 OUNCE CRUNCHY PEANUT BUTTER
    Category
    Food
    Distribution
    49 states
  • SevereFDA (Food)·F-1122-2022·2022-06-08

    JIF Creamy Peanut Butter Recalled for Potential Salmonella Contamination

    The JM Smucker Company is recalling 20,021 cases of JIF 340-gram Creamy Peanut Butter due to potential Salmonella contamination. Affected products distributed nationwide should not be consumed; consumers should discard or return them.

    Product
    JIF 340 GRAM CREAMY PEANUT BUTTER MEXICO
    Category
    Food
    Distribution
    49 states
  • SevereFDA (Drugs)·D-0992-2022·2022-06-08

    Anagrelide Capsules Recalled Due to Failed Dissolution Specifications

    Teva Pharmaceuticals is recalling Anagrelide Capsules USP 0.5 mg nationwide due to failed dissolution specifications discovered during stability testing. The recall involves lot GD01090 (expired May 2022).

    Product
    Anagrelide Capsules USP, 0.5 mg, 100-count bottles, Rx Only, Manufactured in India For: TEVA PHARMACEUTICALS USA, Inc., North Wales, PA 19454. NDC 0172-5241-60.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1113-2022·2022-06-08

    JIF 40 Ounce Natural Honey Recalled Due to Salmonella

    The JM Smucker Company is recalling JIF 40 Ounce Natural Honey due to potential Salmonella contamination. Affected products have lot codes 1274425 or 2140425 with best-by dates from October 2022 to May 2023.

    Product
    JIF 40 OUNCE NATURAL HONEY
    Category
    Food
    Distribution
    49 states
  • SevereFDA (Food)·F-1148-2022·2022-06-08

    Walnut Creek Chocolate Assorted Creams Recalled for Potential Salmonella

    Walnut Creek Chocolate Co Inc is recalling Assorted Creams in 8oz and 16oz boxes due to potential Salmonella contamination. The recall affects 392 units distributed across multiple states.

    Product
    Assorted Creams packaged in 8oz and 16oz boxes
    Category
    Food
    Distribution
    29 states
  • SevereFDA (Food)·F-1139-2022·2022-06-08

    Fudge Sampler Recalled for Potential Salmonella Contamination

    Walnut Creek Chocolate Co Inc recalls Fudge Sampler products due to potential Salmonella contamination. The recall involves 406 units distributed across 29 states.

    Product
    Fudge Sampler
    Category
    Food
    Distribution
    29 states
  • SevereFDA (Food)·F-1150-2022·2022-06-08

    Dutch Delight Peanut Butter Cups recalled for potential Salmonella contamination

    Walnut Creek Chocolate Co Inc is recalling Dutch Delight Peanut Butter Cups due to potential Salmonella contamination. The recall affects 192 units with specific lot codes distributed across 30 states.

    Product
    Dutch Delight Peanut Butter Cup packaged as 10 piece or 10oz tub
    Category
    Food
    Distribution
    29 states
  • SevereFDA (Food)·F-1136-2022·2022-06-08

    Jason & Mary Large Milk Peanut Butter Cups Recalled for Salmonella

    Walnut Creek Chocolate Co Inc is recalling Jason & Mary Large Milk Peanut Butter Cups due to potential Salmonella contamination. The recall covers 7,747 units distributed across 30 states.

    Product
    Jason & Mary Large Milk Peanut Butter Cup
    Category
    Food
    Distribution
    29 states
  • SevereFDA (Food)·F-1141-2022·2022-06-08

    Graham Peanut Butter Bars Recalled Due to Potential Salmonella Contamination

    Walnut Creek Chocolate Co Inc is recalling Graham Peanut Butter Bars due to potential Salmonella contamination. Affected lot codes are 1320, 1335, 1350, 1342, 1356, 1363, 2012, 2032, 2053, 209, 2103, 2118, 2123, and 2124.

    Product
    Graham Peanut Butter Bars
    Category
    Food
    Distribution
    29 states
  • SevereFDA (Food)·F-1111-2022·2022-06-08

    JIF Peanut Butter Recalled for Potential Salmonella Contamination

    The JM Smucker Company recalls JIF 3/4 ounce peanut butter cases due to potential Salmonella contamination. The recall affects approximately 549,884 cases distributed nationwide.

    Product
    JIF 3/4 OUNCE PEANUT BUTTER PLASTIC CASE
    Category
    Food
    Distribution
    49 states
  • SevereFDA (Food)·F-1107-2022·2022-06-08

    JIF Creamy Peanut Butter Recalled Due to Salmonella Contamination Risk

    The JM Smucker Company is recalling JIF Creamy Peanut Butter in multiple sizes due to potential Salmonella contamination. The recall affects millions of cases distributed to all 50 states.

    Product
    JIF CREAMY PEANUT BUTTER packaged in 18gram, 500gram, 1 kilogram, 1.1oz (120 count)12oz, 16oz, 28oz, 40oz, 48oz, 4lb packaged in twin pack 80oz and 96oz
    Category
    Food
    Distribution
    49 states
  • SevereFDA (Food)·F-1109-2022·2022-06-08

    JIF Natural Crunchy Peanut Butter Recall Due to Salmonella

    The JM Smucker Company is recalling JIF Natural Crunchy Peanut Butter (16oz and 40oz) due to potential Salmonella contamination. Affected products have lot codes 1274425 or 2140425.

    Product
    JIF NATURAL CRUNCHY PEANUT BUTTER packaged in 16oz and 40oz
    Category
    Food
    Distribution
    49 states
  • SevereFDA (Food)·F-1108-2022·2022-06-08

    Jif Crunchy Peanut Butter Recalled for Potential Salmonella Contamination

    The JM Smucker Company is recalling JIF Crunchy Peanut Butter in multiple package sizes due to potential Salmonella contamination. The recall affects 1,567,672 cases distributed nationwide.

    Product
    JIF CRUNCHY PEANUT BUTTER packaged in 500 gram, 1 kilogram, 16oz, 28oz, 40oz, 48oz packaged in twin pack 80oz and 96oz
    Category
    Food
    Distribution
    49 states
  • SevereFDA (Devices)·Z-1138-2022·2022-06-08

    In-Line Ventilator Adaptor Recall: Risk of Reduced Oxygenation or Barotrauma

    Baxter Healthcare is recalling 259 in-line ventilator adaptors due to potential risk of reduced oxygenation or barotrauma when used with Volara systems in home care settings.

    Product
    In-Line ventilator adaptor
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1128-2022·2022-06-08

    JIF Peanut Butter To Go Recalled Due to Salmonella Risk

    The JM Smucker Company is recalling JIF 1.5 oz Crunchy Peanut Butter To Go packages due to potential Salmonella contamination. Consumers should not consume affected product.

    Product
    JIF 1.5 oz CRUNCHY PEANUT BUTTER TO GO packaged in 8 count cases
    Category
    Food
    Distribution
    49 states
  • SevereFDA (Food)·F-1114-2022·2022-06-08

    JIF Natural Creamy Peanut Butter recalled for potential Salmonella contamination

    The JM Smucker Company is recalling JIF Natural Creamy Peanut Butter in multiple package sizes due to potential Salmonella contamination. The recall affects 553,007 cases distributed nationwide.

    Product
    JIF NATURAL CREAMY PEANUT BUTTER packaged in 16oz, 28oz, 40oz, 48oz
    Category
    Food
    Distribution
    49 states
  • SevereFDA (Food)·F-1127-2022·2022-06-08

    JIF Light Creamy Peanut Butter recalled for potential Salmonella contamination

    The JM Smucker Company is recalling JIF Light Creamy Peanut Butter due to potential Salmonella contamination. Affected products were distributed nationwide; consumers should verify lot codes and best-by dates and refrain from consuming the product.

    Product
    JIF LIGHT CREAMY PEANUT BUTTER packaged in 500 gram and 1 kilogram
    Category
    Food
    Distribution
    49 states
  • SevereFDA (Food)·F-1116-2022·2022-06-08

    JIF Peanut Butter Recalled Due to Potential Salmonella Contamination

    The JM Smucker Company is recalling 67,504 cases of JIF 33.5 oz No Added Sugar Creamy Peanut Butter due to potential Salmonella contamination. Affected products have lot codes 1274425 or 2140425 with best-by dates from 10/01/22 to 05/20/23.

    Product
    JIF 33.5 OUNCE NO ADDED SUGAR CREAMY PEANUT BUTTER
    Category
    Food
    Distribution
    49 states
  • SevereFDA (Food)·F-1146-2022·2022-06-08

    Peanut Butter Pretzel Cluster Recalled for Potential Salmonella Contamination

    Walnut Creek Chocolate Co Inc is recalling Jason & Mary Peanut Butter Pretzel Cluster due to potential Salmonella contamination. The recalled product was distributed across 29 states.

    Product
    Jason & Mary Peanut Butter Pretzel Cluster
    Category
    Food
    Distribution
    29 states
  • SevereFDA (Food)·F-1129-2022·2022-06-08

    JIF Creamy Peanut Butter To Go Recalled for Potential Salmonella Contamination

    JIF 1.5 oz Creamy Peanut Butter To Go products manufactured by The JM Smucker Company may contain Salmonella. The recall affects 330,528 cases distributed to all 50 states.

    Product
    JIF 1.5 oz NATURAL CREAMY PEANUT BUTTER TO GO packaged in 8 and 36 count cases
    Category
    Food
    Distribution
    49 states
  • SevereNHTSA·22V405000·2022-06-08

    Commercial trucks recalled for defective steering gears

    Daimler Trucks is recalling 2022-2023 Freightliner MT45, MT45G, and Cascadia trucks because steering gears may have been incorrectly assembled and could fracture, causing loss of steering control.

    Product
    FCCC — FCCC, FREIGHTLINER MT45G, MT45, CASCADIA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1131-2022·2022-06-08

    Dierbergs Kitchen spiral pasta salad mislabeled; undeclared egg allergen

    Dierbergs Kitchen Fresh Garden Spiral Pasta Salad is mislabeled as Garden Spiral Pasta but actually contains Broccoli Cheddar Pasta, which contains undeclared egg allergen. Consumers with egg allergies should not consume this product.

    Product
    Dierbergs Kitchen Fresh Garden Spiral Pasta Salad Size: 12oz and 2 lb UPC: 231145703543 Sell By May 31, 22 Sell By Date: 05/31/22 Fresh Garden Spiral Pasta Salad Size: 2LB Family Pack UPC: 231145311625 Sell By Date: 05/31/22
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·F-1119-2022·2022-06-08

    JIF Natural Creamy Peanut Butter with Honey Recalled for Salmonella Risk

    The JM Smucker Company is recalling JIF 16 Ounce Natural Creamy Peanut Butter with Honey due to potential Salmonella contamination. The affected product was distributed across all U.S. states.

    Product
    JIF 16 OUNCE NATURAL CREAMY PEANUT BUTTER HONEY
    Category
    Food
    Distribution
    49 states
  • SevereFDA (Food)·F-1138-2022·2022-06-08

    Assorted Chocolate Gift Boxes Recalled for Potential Salmonella Contamination

    Walnut Creek Chocolate Co Inc is recalling 8,139 units of Assorted Chocolate Gift Boxes due to potential Salmonella contamination. The recall affects 30 states.

    Product
    Assorted Chocolate Gift Boxes packaged in 4oz ,8oz, 16oz, and 32oz boxes
    Category
    Food
    Distribution
    29 states
  • SevereFDA (Food)·F-1140-2022·2022-06-08

    Milk Peanut Butter Cups Recalled for Potential Salmonella Contamination

    Walnut Creek Chocolate Co Inc is recalling Milk Peanut Butter Cups due to potential Salmonella contamination. The FDA Class I recall affects 3,276 units distributed across 30 US states.

    Product
    Milk Peanut Butter Cups
    Category
    Food
    Distribution
    29 states
  • SevereFDA (Food)·F-1143-2022·2022-06-08

    Buckeye Fudge Recalled Due to Potential Salmonella Contamination

    Walnut Creek Chocolate Co Inc is recalling Buckeye Fudge products due to potential Salmonella contamination. The recall affects 724 units distributed across 30 states.

    Product
    Buckeye Fudge packaged in 8oz tub, 5lb loaf, 4lb tray
    Category
    Food
    Distribution
    29 states
  • SevereFDA (Food)·F-1124-2022·2022-06-08

    JIF Reduced Fat Peanut Butter Recalled for Potential Salmonella Contamination

    JIF 454-gram reduced fat creamy peanut butter sold nationwide has been recalled due to potential Salmonella contamination. The FDA Class I recall affects 2,880 cases distributed across all 50 states.

    Product
    JIF 454 GRAM REDUCED FAT CREAMY PEANUT BUTTER MEXICO
    Category
    Food
    Distribution
    49 states
  • SevereFDA (Food)·F-1115-2022·2022-06-08

    JIF Natural Creamy Peanut Butter Recalled for Salmonella Contamination

    The JM Smucker Company is recalling certain JIF Natural Creamy peanut butter products distributed nationwide due to potential Salmonella contamination. Consumers should not consume the affected products.

    Product
    JIF NATURAL CREAMY packaged as a twin pack in 80oz and 96oz packaged as a squeezable pouch in 13oz
    Category
    Food
    Distribution
    49 states
  • SevereFDA (Food)·F-1123-2022·2022-06-08

    JIF Peanut Butter Recalled for Potential Salmonella Contamination

    JIF 454 gram crunchy peanut butter from specific lot codes is being recalled due to potential Salmonella contamination. Affected products were distributed nationwide.

    Product
    JIF 454 GRAM CRUNCHY PEANUT BUTTER MEXICO
    Category
    Food
    Distribution
    49 states
  • SevereFDA (Food)·F-1133-2022·2022-06-08

    Mary's Harvest Celery Peanut Butter Cups Recalled for Potential Salmonella

    Mary's Harvest Celery Peanut Butter Cups (7.5 oz. cups) with Use By dates from 05/15/2022 to 05/31/2022 are recalled in Oregon and Washington due to potential Salmonella contamination.

    Product
    Mary's Harvest brand, Celery Peanut Butter Cup G&G, net wt. per cup 7.5 oz., UPC 8 87241 79672 1
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Food)·F-1110-2022·2022-06-08

    JIF Crunchy Peanut Butter Recalled for Potential Salmonella Contamination

    The FDA is recalling 750 cases of JIF 12 ounce Crunchy Peanut Butter International due to potential Salmonella contamination. Consumers should not consume affected products with the specified lot codes and Best By dates.

    Product
    JIF 12 OUNCE CRUNCHY PEANUT BUTTER INTERNATIONAL
    Category
    Food
    Distribution
    49 states
  • SevereFDA (Food)·F-1121-2022·2022-06-08

    JIF Creamy Peanut Butter To Go Recalled Due to Salmonella Risk

    The JM Smucker Company is recalling JIF 1.5 oz and 31.25 gram Creamy Peanut Butter To Go packages due to potential Salmonella contamination. These products were distributed to all 50 states.

    Product
    JIF 1.5 oz and 31.25 gram CREAMY PEANUT BUTTER TO GO packaged in 3, 8, 36, and 96 count cases
    Category
    Food
    Distribution
    49 states
  • HighFDA (Devices)·Z-1206-2022·2022-06-08

    Medtronic cardiac catheter system recalled due to sterility barrier defect

    Medtronic recalls its C304-HIS cardiac catheter device due to potential sterility barrier defects in certain manufacturing lots. Approximately 1,385 devices distributed worldwide were affected.

    Product
    The C304-HIS device features a guide wire to access the vein, a valve to reduce blood loss during the implant procedure, a deflectable catheter to introduce a transvenous device, a catheter dilator to facilitate deflectable catheter passage, and a guide catheter slitter to remove
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1152-2022·2022-06-08

    Busse Single Shot Epidural Tray recalled for test method validation uncertainty

    Busse Hospital Disposables is recalling Single Shot Epidural Trays nationwide due to uncertainty about the adequacy of test method validation used to manufacture swab components. The FDA classified this as a Class II recall.

    Product
    Single Shot Epidural Tray Catalog 1292
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1225-2022·2022-06-08

    Hip Stem Prosthetic Missing Plasma Coating in Manufacturing Lot

    MicroPort Orthopedics is recalling one manufacturing lot of PROFEMUR PLASMA Z CLASSIC hip stem prosthetics due to missing plasma-spray coating in the proximal region of the implant stem.

    Product
    PROFEMUR PLASMA Z CLASSIC STEM SIZE 7 STANDARD SHORT NECK
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1217-2022·2022-06-08

    MEDLINE Enzymatic Cleaning Sponges Recalled Due to Microbial Contamination

    MEDLINE Polyurethane Foam Enzymatic Cleaning Sponges (REF DYK1000TSE) are being recalled due to microbial contamination identified on certain lots. The affected product was distributed in the US and Panama.

    Product
    MEDLINE Polyurethane Foam Enzymatic Cleaning Sponge, REF DYK1000TSE
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-1166-2022·2022-06-08

    FDA Recalls CVC Dressing Change Kit Due to Manufacturing Validation Uncertainty

    Busse Hospital Disposables is recalling CVC Dressing Change Kits nationwide due to uncertainty about test method validation during manufacturing. Affected swab products may not have been adequately validated for sterility and efficacy.

    Product
    CVC Dressing Change Kit Catalog Number: 2491R1
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·22V404000·2022-06-08

    2020-2022 Porsche Taycan center screen display malfunction increases crash risk

    Porsche is recalling 2020-2022 Taycan vehicles for a software error causing the center screen and touch panel to go black or flicker. This blocks the driver's view of rear-view camera functions, increasing crash risk.

    Product
    PORSCHE — PORSCHE TAYCAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1155-2022·2022-06-08

    Swab Drug Products Recalled Due to Manufacturing Validation Uncertainty

    Convenience kits containing swab/swabstick drug products are being recalled due to uncertainty about whether test methods used during manufacturing adequately validated the products. Affected products include 80 units distributed nationwide.

    Product
    Epidural Tray Catalog 1577
    Category
    Drug
    Distribution
    Distributed nationwide

Looking for a different month? Back to 2022.