Hawaii recalls

Sold nationwide. AvKARE is recalling one lot of fludrocortisone acetate 0.1 mg tablets because testing found impurity or degradation levels above required limits. The recall covers lot 48353 (expiration 10/31/2026) in 50-tablet unit-dose cartons, NDC 50268-330-15, distributed nationwide. No injuries have been reported.

Moderate·FDA·Oct 30, 2026·AvKARE

Sold nationwide. Par Health USA is recalling certain lots of Brevital Sodium (methohexital sodium) for injection, a 500 mg multiple-dose vial sold in the US and Canada. The vials may contain particles identified as cellulose. No injuries have been reported.

Serious·FDA·Oct 30, 2026·Paragon 28

Sold nationwide. ArjoHuntleigh Polska is recalling about 8,780 Carevo height-adjustable shower trolleys, Model BAC1111-01. The side support panel can open unintentionally if the handles are not fully locked and extra force is applied during patient handling, which could cause a patient to fall and be seriously injured.

Moderate·FDA·Oct 29, 2026·Arjohuntleigh

Sold nationwide. Stryker Leibinger is recalling Precision Pointer Electromagnetic devices because the pointer tube can crack at a laser-welded joint during use. If that happens, loose parts could fall out while the device is inside a patient. No injuries have been reported.

Moderate·FDA·Oct 29, 2026·Stryker

Sold nationwide. Boston Scientific is recalling certain Nalu TD2 Therapy Discs and TD2 Patient Kits used with the Nalu Neurostimulation System. A firmware problem can cause the disc to try to restart and then fail, so it stops working. If no backup disc is available, the implanted pulse generator may also stop working, which could leave pain signals unblocked. No injuries have been reported.

Moderate·FDA·Oct 29, 2026·Boston Scientific

Sold nationwide. Novadoz Pharmaceuticals is recalling about 13,296 bottles of 1,000-count atorvastatin calcium 40mg tablets distributed nationwide. Some bottles may contain other tablets or capsules that are not atorvastatin. No injuries have been reported.

Moderate·FDA·Oct 29, 2026·MSN Laboratories

Sold nationwide. Brandywine Pharmaceuticals is recalling one lot of theophylline extended-release tablets, 100 mg, because stability testing for the product was interrupted at a third-party lab. Stability testing checks whether a medicine stays within its quality standards over time. No injuries have been reported.

Moderate·FDA·Oct 29, 2026·Brandywine Pharmaceuticals2 products

Sold nationwide. Meitheal Pharmaceuticals is recalling about 121,800 vials of Vecuronium Bromide for Injection, 10 mg, because the labels lack a required warning or prescription legend. No injuries have been reported. The FDA classified this as a Class III recall, which means it is unlikely to cause serious harm.

FDA·Oct 29, 2026·Meitheal Pharmaceuticals2 products

Sold nationwide. Direct Rx is recalling 493 jars of Lidocaine Ointment USP, 5.0%, 50g, because the product may contain less lidocaine than its label states. The affected lots are 03AP2511, 30AP2518, 18JU2519, and 18JU2520, with an expiration date of 04/30/2027. The product was distributed nationwide, and no injuries have been reported.

Moderate·FDA·Oct 29, 2026·Direct Rx

Sold nationwide. Longjili Trading is recalling about 50 Pamag Pieeoo twin-XL mattresses. The mattresses do not meet the mandatory federal flammability standard for mattresses, which can lead to serious injury or death from fire. No injuries have been reported.

Serious·CPSC·Oct 29, 2026·Longjili Trading

Sold nationwide. Harkla is recalling about 25,541 children's sensory compression swings in the U.S. because the ceiling hook can separate from its plate, posing a risk of serious fall injury. The company has received 29 reports of hook separation, including 14 injuries such as two concussions and a broken arm. The swings were sold online and in stores from March 2020 through December 2025.

Serious·CPSC·Oct 29, 2026·Harkla

Sold nationwide. Yinklev is recalling about 32,791 Jocoevol 6-drawer dressers sold on Amazon.com from December 2024 through July 2026 for about $160. The dressers can tip over if they are not anchored to the wall, posing risks of serious injury or death to children. They also do not meet a mandatory federal safety standard for clothing storage units.

Serious·CPSC·Oct 29, 2026·Yinklev

Sold nationwide. RootStim recalled about 11,000 minoxidil hair regrowth treatment bottles sold on Amazon from August 2025 through February 2026. The bottles are not child-resistant, which federal packaging rules require for minoxidil, so young children could open and swallow the product. No injuries have been reported.

Serious·CPSC·Oct 29, 2026·RootStim

Sold nationwide. HAIARA W5 PRO power banks sold on Amazon.com by Mitrytech are being recalled because the lithium battery can explode and ignite. The recall covers power banks with no date code printed on the side. About 11,000 units were sold for $18 to $22 from May 2025 through September 2026, and the company has received 600 reports of fire and other heat-related incidents, including three burn injuries.

Serious·CPSC·Oct 29, 2026·HAIARA

Sold nationwide. Bodum USA is recalling about 5.9 million French press coffee makers with replaceable glass carafes. The glass carafe can break during use, especially if it is cracked or damaged or if a metal spoon is used to stir the coffee. The company has received 70 reports of carafes breaking, including 48 reports of burns.

Serious·CPSC·Oct 29, 2026·Bodum

Sold nationwide. DREO is recalling about 338,800 DR-HSH015 space heaters in the U.S. because they can overheat and ignite. The recall covers units made from April 2025 through January 2026, with the manufacture date and model number on a label on the underside. DREO has received 17 reports of the heaters catching fire, including three cases of property damage and one hand burn injury.

Serious·CPSC·Oct 29, 2026·DREO

Sold nationwide. Ariston Canada, formerly NTI Boilers, is recalling certain NTI and HTP gas boilers. A cracked condensate dish can let unburned gas build up inside the sealed cabinet, and if that gas ignites, the front cover can suddenly come off. The company has received 34 reports of the dish breaking, including three reports of the cover detaching, and one technician was seriously injured.

Serious·CPSC·Oct 29, 2026·Ariston

Sold nationwide. Whatever Works is recalling about 8,709 microwave grillers because they can overheat and ignite. The company has received three reports of grills catching fire, and no injuries have been reported. The grills were sold on Whateverworks.com from January 2025 through June 2026 for about $22.

Serious·CPSC·Oct 29, 2026·Whatever Works

Sold nationwide. SOOWERY is recalling about 138 8-drawer fabric dressers sold on Amazon from December 2025 through August 2026 for about $106. The dressers can tip over if they are not anchored to the wall, which can cause serious injury or death to children, and they do not meet a mandatory federal safety standard. No injuries have been reported.

Serious·CPSC·Oct 29, 2026·SOOWERY

Sold nationwide. PILLANI is recalling about 25,762 U-shaped nursing pillows sold on Amazon from April through September 2026. The pillows violate mandatory federal safety standards because they can obstruct an infant's breathing, which poses a serious risk of injury or death from suffocation. No injuries have been reported.

Serious·CPSC·Oct 29, 2026·Pillani

Sold nationwide. Fashion Brand Apparel is recalling about 300 QZH.DUAO children's pajama sets sold on Amazon.com from February through July 2026 for about $23. The sets do not meet mandatory federal safety standards for children's sleepwear, so they can pose a risk of serious burn injuries. No injuries have been reported.

Serious·CPSC·Oct 29, 2026·Fashion Brand Apparel

Sold nationwide. Pentax Medical is recalling five products: four PENTAX Medical ultrasound endoscope models and the PENTAX Medical OS-H5 water bottle assembly, about 3,140 units in total. The agency's warning labeling was updated to say users must make sure deaerated sterile water is in the assembly before and during procedures. No injuries have been reported.

Moderate·FDA·Oct 28, 2026·Pentax5 products

Sold nationwide. Abiomed is recalling 900 Impella heart pump controllers in three products: Automated Impella Controller, Impella Optical Controller, and Impella Connect Optical AIC. The units need hardware, firmware, or software updates found during a review of servicing records. Possible problems include the controller failing to recognize the purge cassette, a sticking push button that can cause loss of console control, start-up failure, and a software defect that can show incorrect negative pressure readings. No injuries have been reported.

Serious·FDA·Oct 28, 2026·Abiomed3 products

Sold nationwide. American Regent Inc. is recalling one lot of BetaVet, a betamethasone injectable suspension for intra-articular use in horses, sold in 5 mL single-dose vials. The vial crimps or seal may be loose or defective, which could affect the container's integrity. The recall covers lot 26038L2C1 (expires July 2027) and was distributed nationwide; no injuries have been reported.

Moderate·FDA·Oct 28, 2026·BetaVet

Sold nationwide. JXK Enterprises, Inc. is voluntarily recalling Boner Bears Chocolate, Lot #BB21125, sold as a male enhancement product. FDA lab testing found sildenafil, the active ingredient in the prescription drug Viagra, which is not listed on the label. The product was sold nationwide online through www.elyxr.com.

Serious·FDA·Oct 28, 2026·Boner Bears

Sold nationwide. GF Blends is recalling three gluten-free baking mixes because they may contain wheat gluten that is not listed on the label. The products are sold as Gluten Free Truly AIP flour, bread mix and the EAT G.A.N.G.S.T.E.R pizza crust and flat bread mix, and were sold nationwide online at eatgangster.com, trulyaip.com and Amazon.com. No injuries have been reported.

Serious·FDA·Oct 28, 2026·Gluten Free Truly AIP3 products

Sold nationwide. Eagle Pharma Outsourcing is recalling two compounded IV infusion products nationwide: phenylephrine HCl (100 mg in 250 mL saline, 50 containers) and oxytocin (30 units in 500 mL saline, 5 containers). The company cannot assure that the products are sterile. No injuries have been reported.

Moderate·FDA·Oct 28, 2026·Eagle Pharma Outsourcing2 products

Sold nationwide. AvKARE is recalling one lot of amitriptyline hydrochloride 10 mg tablets because they failed dissolution specifications. The recall covers 3,534 cartons of 50-count unit dose cards distributed nationwide. No injuries have been reported.

Moderate·FDA·Oct 28, 2026·AvKARE

Sold nationwide. Medtronic is recalling three CareLink SmartSync products, including the programmer, RF head patient connector and Device Manager app, because a software problem can cause an inaccurate displayed longevity estimate for implanted pulse generators. No injuries have been reported. The recall covers about 61,000 units distributed worldwide.

Moderate·FDA·Oct 27, 2026·Medtronic3 products

Sold nationwide. BioMerieux is recalling a limited number of EMAG nucleic acid sample preparation instruments used in clinical labs. After updating to firmware SP4 Patch 2, a random software error (Error 10003, Heater timeout) can cause delayed or no results when analyzing clinical samples. No injuries have been reported.

Moderate·FDA·Oct 27, 2026·bioMérieux