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Consumer Product Recalls
127,244 recalls from the U.S. Consumer Product Safety Commission, newest first.
March 5, 2026Vehicle EquipmentNHTSA
Webasto Electrical System recall
Hazard: Battery failure can cause a loss of drive power, increasing the risk of a crash. Battery failure can also increase the risk of a fire.

March 5, 2026ToysCPSC
Cubimana Island Storm 3 In 1 Building Sets Recalled Due to Risk of Serious Injury or Death from Battery Ingestion; Violates Mandatory Standard for Toys; Sold on Amazon by RBS Toys
Hazard: The Island Storm Building Sets violate the mandatory safety standard for toys because the battery compartment within the LED light piece contains button cell batteries that can be easily accessed by children. When button cell or coin batteries are swallowed, the ingested batteries can cause serious injuries, internal chemical burns and death.

March 5, 2026Children's ProductsCPSC
HALO Dream Recalls Magic Sleepsuits Due to Choking Hazard
Hazard: The zipper head can detach from certain sleepsuits, posing a choking hazard to infants.

March 5, 2026OtherCPSC
Tomum Minoxidil Hair Serum Spray Bottles Recalled Due to Risk of Serious Injury or Death from Child Poisoning; Violates Mandatory Standard for Child-Resistant Packaging; Distributed by Belleka
Hazard: The hair serum contains minoxidil, which must be in child-resistant packaging as required by the Poison Prevention Packaging Act. The hair serum's bottles are not child-resistant, posing a risk of serious injury or death from poisoning if the contents are swallowed by young children.

March 5, 2026Children's ProductsCPSC
Unique Brands Com Recalls Forever 21 Pajama Pants Due to Risk of Serious Injury or Death from Burn Hazard; Violates Mandatory Flammability Standards for Children's Sleepwear
Hazard: The recalled children's pajama pants violate the mandatory standards for flammability of children's sleepwear, posing a burn hazard and risk of serious injury or death to children.
March 4, 2026Medical DevicesFDA
Remel, Inc recalls Campy CVA Medium 100/PK, R01272
Hazard: Customer complaints report low to no recovery of Campylobacter Jejuni ATCC 33291 on identified lot of medium.
March 4, 2026Medical DevicesFDA
Medtronic Perfusion Systems recalls Octopus Nuvo Tissue Stabilizer, disposable tissue stabilization system, Product Number TSMICS1
Hazard: During the manufacturing, Medtronic personnel identified an assembly issue where the tubing was incorrectly positioned. The short tube was attached to the bottom of the canister, and the long tube was attached to the top, contrary to the intended design.
March 4, 2026Medical DevicesFDA
Agiliti Health - Ellis recalls Adapt Pump, Model/Catalog Number: 61600200-Adapt Pump, component of Adapt support surfaces (Adapt Air, Adapt Air EX, Ada
Hazard: Agiliti identified an issue where the Adapt Pump (61600200-Adapt Pump) supplied with all Adapt Line support surfaces does not re-engage the Microclimate Management function after using the Autofirm function for 10 minutes. This issue only occurs when the 10-minute timer is allowed to elapse after the Autofirm button is pressed after initial setup, and it only affects the Microclimate Management function.
March 4, 2026Medical DevicesFDA
Medline Industries, LP recalls Convenience kits containing Tego Connectors Medline DIALYSIS DRSNG CHNG SKU DYNDC3167
Hazard: 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.
March 4, 2026Medical DevicesFDA
Medline Industries, LP recalls Convenience kits containing Tego Connectors: Medline DIALYSIS DRESSING CHANGE SKU EBSI1498 Medline DIALYSIS DRESS
Hazard: 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.
March 4, 2026Medical DevicesFDA
Medline Industries, LP recalls Medline kits containing Tego Connectors Medline APHERESIS SUBQPORT ACCESS KIT SKU DYNDA2705 Medline CENTRAL LINE
Hazard: 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.
March 4, 2026Medical DevicesFDA
Medline Industries, LP recalls Convenience kits used for dialysis maintenance Medline ADD A CATH DIALYSIS KIT SKU ECVC8415A Centurion CENTRAL LI
Hazard: 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.
March 4, 2026Medical DevicesFDA
Medline Industries, LP recalls Medline Kits containing Tego Connectors Medline DIALYSIS ON/OFF KIT SKU EBSI1746
Hazard: 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.
March 4, 2026Medical DevicesFDA
Medline Industries, LP recalls Medline Kits containing Tego Connectors: Medline IR Pack, SKU DYNJ67205C Medline NO CATHETER DIALYSIS INSERTION, SKU C
Hazard: 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.
March 4, 2026Medical DevicesFDA
Edermy LLC recalls PIE PAK Models: P2HC-A, P2HC-S, P2HC
Hazard: Lack of 510K clearance
March 4, 2026Medical DevicesFDA
Edermy LLC recalls PIE Trolley System Model: 2005
Hazard: Lack of 510K clearance
March 4, 2026Medical DevicesFDA
Encore Medical, LP recalls Brand Name: Reverse Shoulder Prosthesis (RSP) Product Name: RSP STANDARD HUMERAL SOCKET INSERT, 36MM, HXe-plus Model/C
Hazard: Knee and Humeral socket implants contain incorrect labeling.
March 4, 2026Medical DevicesFDA
Encore Medical, LP recalls Brand Name: EMPOWR 3D KNEE Product Name: EMPOWR 3D KNEE INS, 7L 16MM, VE Model/Catalog Number: 341-16-707
Hazard: Knee and Humeral socket implants contain incorrect labeling.
March 4, 2026Medical DevicesFDA
Encore Medical, LP recalls Brand Name: Reverse Shoulder Prosthesis (RSP) Product Name: RSP HUMERAL SOCKET INSERT, 32MM +4MM, STANDARD HXe-plus Mo
Hazard: Knee and Humeral socket implants contain incorrect labeling.
March 4, 2026Medical DevicesFDA
Olympus Corporation of the Americas recalls Olympus Resection Sheath. Model No. A2666T. for endoscopic diagnosis and treatment in urological applications.
Hazard: Complaints of the ceramic tip of the resection sheath breaking have been received.
March 4, 2026Medical DevicesFDA
Olympus Corporation of the Americas recalls Olympus Inner Sheath. Model No. A2642. for endoscopic diagnosis and treatment in urological applications.
Hazard: Complaints of the ceramic tip of the resection sheath breaking have been received.
March 4, 2026Medical DevicesFDA
Olympus Corporation of the Americas recalls Olympus Inner Sheath. Model No. A2641. for endoscopic diagnosis and treatment in urological applications.
Hazard: Complaints of the ceramic tip of the resection sheath breaking have been received.
March 4, 2026Medical DevicesFDA
Olympus Corporation of the Americas recalls Olympus Sheath, 10 Fr. Model No. A37004A. for endoscopic diagnosis and treatment in urological applications.
Hazard: Complaints of the ceramic tip of the resection sheath breaking have been received.
March 4, 2026Medical DevicesFDA
Olympus Corporation of the Americas recalls Olympus Inner Sheath 21 Fr. Model No. A2660T. for endoscopic diagnosis and treatment in urological applications.
Hazard: Complaints of the ceramic tip of the resection sheath breaking have been received.
March 4, 2026Medical DevicesFDA
Olympus Corporation of the Americas recalls Olympus Resection Sheath; Model No. A2666. Resection sheath for urologic applications.
Hazard: Complaints of the ceramic tip of the resection sheath breaking have been received.
March 4, 2026Medical DevicesFDA
Olympus Corporation of the Americas recalls Olympus Inner Sheath, Long; Model No. WA22017T. Inner sheath for urological and gynecological applications.
Hazard: Complaints of the ceramic tip of the resection sheath breaking have been received.
March 4, 2026Medical DevicesFDA
Olympus Corporation of the Americas recalls Olympus Inner Sheath, Long; Model No. WA22017A. Inner sheath for urological and gynecological applications.
Hazard: Complaints of the ceramic tip of the resection sheath breaking have been received.
March 4, 2026Medical DevicesFDA
Olympus Corporation of the Americas recalls Olympus Inner Sheath. Model No. A4741. for endoscopic diagnosis and treatment in gynecological applications.
Hazard: Complaints of the ceramic tip of the resection sheath breaking have been received.
March 4, 2026Medical DevicesFDA
Olympus Corporation of the Americas recalls Olympus Resection Sheath, 8 mm. Model No. A42011A. Resection sheath for gynecological applications.
Hazard: Complaints of the ceramic tip of the resection sheath breaking have been received.
March 4, 2026Medical DevicesFDA
Olympus Corporation of the Americas recalls Olympus Inner Sheath; Model No. A2660. for endoscopic diagnosis and treatment in urological applications.
Hazard: Complaints of the ceramic tip of the resection sheath breaking have been received.