Oklahoma recalls

First Aid Only BZK Antiseptic Towelettes (50-count packages) are being recalled because the manufacturer did not follow required quality and safety procedures during production. The recall affects specific lot numbers distributed nationwide. No injuries have been reported.

First Aid Only BZK Antiseptic Towelettes have been recalled due to manufacturing quality control deviations. The FDA determined that certain lots did not meet required manufacturing standards. No injuries have been reported to date.

Teva Pharmaceuticals is recalling specific lots of metoprolol succinate extended-release 200 mg tablets because they failed to meet dissolution specifications—meaning the tablets may not break down and release the medication properly in your body. This could affect how well the blood pressure medication works. No injuries have been reported.

Teva Pharmaceuticals is recalling specific batches of Metoprolol Succinate Extended-Release 100 mg tablets because they may not dissolve properly in the body. This means the medication may not work as intended. The recall affects bottles with lot numbers ending in J251 or J252 and expiration dates of 12/2026.

Teva Pharmaceuticals is recalling certain batches of Metoprolol Succinate Extended-Release 50 mg tablets because they may not dissolve properly in the body, which could affect how well the medication works. The affected bottles have specific lot numbers and an expiration date of January 2027. No injuries have been reported.

Teva Pharmaceuticals is recalling specific lots of Metoprolol Succinate Extended-Release 25 mg tablets because they failed to meet dissolution specifications—meaning the tablets may not break down and release the medication properly in your body. This could result in the drug not working as intended. No injuries have been reported.

The Cubimana Island Storm 3 In 1 Building Set (model HG1004) contains an LED light piece with an easy-to-open battery compartment holding button cell batteries. Children can access and swallow these batteries, which can cause serious internal burns and death.

The zipper head on certain HALO Magic Sleepsuits can detach, creating a choking hazard for infants. HALO Dream has received 15 reports of zipper heads coming off, though no injuries have been reported yet. The recall affects sleepsuits sold between September 2025 and February 2026 with batch codes PO30592, PO30641, or PO30685.

Tomum Minoxidil Hair Growth Treatment spray bottles do not have child-resistant caps as required by law. If a young child swallows the contents, it can cause serious injury or death. The product was sold online from March through September 2025.

Forever 21 Kids Disney Mickey Mouse pajama pants in sizes 5/6 through 13/14 fail to meet federal flammability standards for children's sleepwear. The fabric can catch fire and burn more easily than safe sleepwear should, posing a serious burn risk to children.

Remel's Campy CVA Medium (lot R01272, UDI 848838001055) is not reliably recovering Campylobacter Jejuni bacteria during laboratory culture testing. Customers reported low to no bacterial growth on this specific lot, which could lead to missed or delayed diagnoses.

Medtronic found a manufacturing error in 2 units of the Octopus Nuvo Tissue Stabilizer where the tubing was installed backwards—the short tube was attached to the bottom and the long tube to the top, opposite of the correct design. This could affect how the device functions during use.

Agiliti Health's Adapt Pump (used in Adapt Air and Adapt Convertible mattresses) has a software issue that prevents the temperature control (Microclimate Management) function from restarting after the Autofirm button is used for 10 minutes during initial setup. This only happens if you let the timer run out without manually stopping it, and it only affects temperature management—not the mattress's air support.

Medline dialysis dressing change convenience kits (SKU DYNDC3167) may contain defective Tego Connectors with silicone seal problems. The seals can dome or tear, which may block fluid flow, cause therapy delays, leak fluids, or allow air or contamination into the bloodstream.

Medline Industries is recalling several dialysis and pheresis dressing change kits because the silicone seals on included Tego Connectors may be damaged, domed, or torn. A damaged seal can prevent blood withdrawal or injection, cause fluid leakage, delay treatment, or allow air or contaminants into the bloodstream.

Affected lots may exhibit issues with the silicone seal on Tego Connectors included in kits. Issues include silicone seal doming and silicone seal tearing. These issues may result in an occluded fluid path identified by the inability of the user to inject or withdraw blood product with a syringe. Damaged seals may also result in delay in therapy or fluid leakage, interruption in therapy, exposure to biological contaminants or air infused into the body.

Medline dialysis kits containing Tego Connectors may have defective silicone seals that can dome or tear. This can block the fluid path, prevent blood withdrawal, cause fluid leaks, interrupt treatment, or allow air and contaminants into the body.

Medline dialysis on/off kits may contain Tego Connectors with defective silicone seals that can dome or tear. This can block the fluid path, prevent blood product injection or withdrawal, cause fluid leakage, delay treatment, or allow air or contaminants into the body.

Medline Industries is recalling two dialysis insertion kits that contain Tego Connectors with defective silicone seals. The seals may dome or tear, which can block fluid flow, cause therapy delays, allow leaks, or introduce air or contamination into the body.

Edermy LLC is recalling PIE PAK models P2HC-A, P2HC-S, and P2HC because they were sold without FDA 510(k) clearance, which is required before medical devices can be marketed in the U.S. The company distributed approximately 11,202 units nationwide. No injuries have been reported.

Edermy LLC's PIE Trolley System Model 2005 was distributed without required FDA 510(k) clearance, which means the device was not reviewed or approved for safety and effectiveness. The FDA has issued a recall affecting 27 units distributed across multiple states.

Encore Medical's RSP Standard Humeral Socket Insert (36mm, HXe-plus model) was distributed with incorrect labeling. About 20 implants from a single lot were affected across multiple states. No injuries have been reported so far.

Encore Medical's EMPOWR 3D Knee implants (model 341-16-707, lot 151T1055A) were distributed with incorrect labeling that could affect proper surgical placement or identification. Fourteen implants were affected across multiple states. No injuries have been reported.

Encore Medical's RSP humeral socket insert (model 509-00-432, lot 385P1263) has incorrect labeling that could cause confusion during surgical implantation. This affects 20 implants distributed across multiple U.S. states. No injuries have been reported.

The ceramic tip on Olympus Resection Sheath Model A2666T can break during use. This device is used in urological procedures. The FDA has determined this poses a risk to patients.

The ceramic tip on Olympus Inner Sheath Model A2642, used in urological endoscopic procedures, can break during use. The FDA has received complaints of this breakage occurring.

Olympus has recalled the Inner Sheath Model A2641, a medical device used in urological procedures. The ceramic tip of the resection sheath can break during use, which may affect the safety and effectiveness of the procedure.

Olympus Corporation is recalling its 10 Fr. Model A37004A endoscopic sheath used in urological procedures because the ceramic tip can break during use. The company has received complaints about this defect. No injuries have been reported.

Olympus has recalled the Inner Sheath 21 Fr. Model No. A2660T, a medical device used in urological procedures. The ceramic tip on the resection sheath can break during use, which could affect the safety and effectiveness of the procedure.

Olympus has recalled its Model A2666 resection sheath, a medical device used in urologic procedures, because the ceramic tip can break during use. The FDA has classified this as a Class II recall affecting all lots of this device.