Archive
857 recalls were announced in June 2022.
Of the 857 recalls this month scored against our rubric, 3% are Critical, 27% are Severe.
Which agencies issued them
Zydot Unlimited recalls 1,150 bottles of Zydot Ultimate Blend detox drink due to undeclared preservatives and food colorants on the label.
GRUVIPA S.L. is recalling CB1102006 BOCATA 120 sandwiches distributed in Florida due to potential insect filth contamination of the finished product.
McKesson is recalling 9 vials of Duraclon (clonidine HCl) injection nationwide due to temperature deviations that violated current Good Manufacturing Practice (cGMP) standards.
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.
McKesson is recalling doxycycline hyclate 100 mg tablets nationwide due to temperature abuse during manufacturing that fails to meet good manufacturing practice standards.
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.
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.
McKesson Medical-Surgical is recalling Azithromycin for Injection 500 mg vials nationwide due to temperature control deviations identified during manufacturing.
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.
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.
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.
McKesson Medical-Surgical is recalling DIPRIVAN (Propofol) injectables nationwide due to temperature abuse during distribution that may have affected product stability. The recall involves 46 cartons.
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.
McKesson Medical-Surgical is recalling Tetracaine Hydrochloride Ophthalmic Solution due to cGMP deviations from temperature abuse. The recall affects 43 cartons distributed nationwide.
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.
McKesson Medical-Surgical is recalling Hydrocortisone Ointment USP 2.5% nationwide due to temperature abuse during distribution that violated manufacturing standards.
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.
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.
McKesson Medical-Surgical is recalling Arzol silver nitrate applicators nationwide due to temperature abuse during manufacturing that may affect product quality.
McKesson Medical-Surgical is recalling MIOSTAT (Carbachol Intraocular Solution) nationwide due to temperature abuse during distribution that may affect medication stability.
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.
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.
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.
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.
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.
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.
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.
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.
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.
Ford is recalling 2021-2022 Mustang Mach-E vehicles because high voltage battery contactors may overheat, potentially causing loss of drive power and increasing crash risk.
Ford is recalling 2022 Transit vehicles because the instrument panel cluster may fail to illuminate gauges and telltales, potentially increasing crash risk.
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.
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.
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.
Chrysler is recalling 2018-2019 Jeep Grand Cherokee and Dodge Durango vehicles because an ABS module malfunction may allow the car to roll away without the brake pedal being applied.
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.
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.
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.
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.
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.
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.
Ferrara is recalling 2021-2023 Inferno and Igniter vehicles because a defective circuit board can cause lighting to fail, increasing crash risk.
Forest River is recalling 2022 Prime Time Crusader and Sanibel fifth wheel travel trailers because step treads may detach, increasing injury risk.
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.
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.
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.
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.
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.
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.
The FDA recalled JIF 16 Ounce Creamy Omega 3 Peanut Butter due to potential Salmonella contamination. Approximately 33,516 cases distributed nationwide are affected.
Walnut Creek Chocolate Co Inc is recalling Peanut Butter Caramel Corn due to potential Salmonella contamination. The recall affects 234 units distributed to multiple U.S. states.
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.
Walnut Creek Chocolate Co Inc is recalling Ritz Peanut Butter due to potential Salmonella contamination. The recall affects 682 units distributed across 29 states.
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.
Walnut Creek Chocolate Co Inc is recalling Assorted Chocolate Heart Boxes due to potential Salmonella contamination. Consumers should not consume the recalled products.
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.
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.
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.
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.
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).
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.
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.
Walnut Creek Chocolate Co Inc recalls Fudge Sampler products due to potential Salmonella contamination. The recall involves 406 units distributed across 29 states.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
The JM Smucker Company is recalling Jif Dark Roast Creamy Peanut Butter due to potential Salmonella contamination. The recall affects 23,635 cases distributed nationwide.
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.
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.
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.
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.
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.
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.
Zero Motorcycles is recalling 2022 SR and SR/F motorcycles because incorrect front brake caliper bolts may damage fork threads, causing the caliper to loosen and reduce braking.
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.
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.
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.
Walnut Creek Chocolate Co Inc is recalling Buckeye Fudge products due to potential Salmonella contamination. The recall affects 724 units distributed across 30 states.
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.
The JM Smucker Company is recalling JIF No Added Sugar Peanut Butter in 15.5-ounce and 46.5-ounce containers distributed nationwide due to potential 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.
JIF 454 gram crunchy peanut butter from specific lot codes is being recalled due to potential Salmonella contamination. Affected products were distributed nationwide.
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.
The JM Smucker Company is recalling JIF 13-ounce Natural Creamy Peanut Butter Squeeze Pouches due to potential Salmonella contamination. Affected products were distributed nationwide.
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.
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.
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.
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.
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.
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.
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.
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.
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.
Looking for a different month? Back to 2022.