Connecticut recalls
3509 federal recalls on file affecting Connecticut - 435 Connecticut-specific plus 3074 nationwide. Sourced from CPSC, FDA, USDA, and NHTSA.
- 2026-03-11FDA-DrugAcmeClass IINationwideStop using Max Packaging antibacterial towelettes
CGMP Deviations
- 2026-03-11FDA-DrugAcmeClass IINationwideStop using recalled BZK Antiseptic Towelettes
CGMP Deviations
- 2026-03-11FDA-DrugAcmeClass IINationwideStop using First Aid Only BZK Antiseptic Towelettes
CGMP Deviations
- 2026-03-11FDA-DrugAcmeClass IINationwideCheck Dukal BZK Antiseptic Towelette lot numbers
CGMP Deviations
- 2026-03-11FDA-DrugAcmeClass IINationwideStop using First Aid Only BZK towelettes
CGMP Deviations
- 2026-03-11FDA-DrugAcmeClass IINationwideStop using First Aid Only BZK Antiseptic Towelettes
CGMP Deviations
- 2026-03-11FDA-DrugTevaClass IINationwideStop using Teva metoprolol succinate 200 mg tablets
Failed Dissolution Specifications
- 2026-03-11FDA-DrugTevaClass IINationwideStop taking Teva Metoprolol Succinate tablets
Failed Dissolution Specifications
- 2026-03-11FDA-DrugTevaClass IINationwideStop using Teva Metoprolol Succinate 50 mg tablets
Failed Dissolution Specifications
- 2026-03-11FDA-DrugTevaClass IINationwideStop using Teva Metoprolol Succinate tablets
Failed Dissolution Specifications
- 2026-03-05CPSCRBS ToysNationwideStop using Cubimana Island Storm building sets
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.
- 2026-03-05CPSCHALONationwideStop using HALO Dream Magic Sleepsuit
The zipper head can detach from certain sleepsuits, posing a choking hazard to infants.
- 2026-03-05CPSCTOMUMNationwideSecure Tomum hair serum away from children immediately
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.
- 2026-03-05CPSCUnique BrandsNationwideStop using Forever 21 Kids pajama pants
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.
- 2026-03-04FDA-DeviceRemelClass IINationwideStop using Remel Campy CVA Medium lot R01272
Customer complaints report low to no recovery of Campylobacter Jejuni ATCC 33291 on identified lot of medium.
- 2026-03-04FDA-DeviceMedtronicClass IINationwideCheck Medtronic Octopus Nuvo Tissue Stabilizer lot 0232837110
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.
- 2026-03-04FDA-DeviceAgiliti HealthClass IINationwideCheck your Agiliti Adapt Pump settings
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.
- 2026-03-04FDA-DeviceMedlineClass IINationwideStop using Medline dialysis dressing change kits
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.
- 2026-03-04FDA-DeviceMedlineClass IINationwideStop using recalled dialysis dressing kits
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.
- 2026-03-04FDA-DeviceMedlineClass IINationwideMedline kits containing Tego Connectors Medline APHERESIS SUBQPORT ACCESS KIT SKU DYNDA2705 Medline CENTRAL LINE INSERTION SKU DYNJ63347A
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.
- 2026-03-04FDA-DeviceMedlineClass IINationwideStop using affected Medline dialysis kits
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.
- 2026-03-04FDA-DeviceMedlineClass IINationwideStop using Medline dialysis on/off kits (SKU EBSI1746)
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.
- 2026-03-04FDA-DeviceMedlineClass IINationwideStop using affected Medline dialysis kits
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.
- 2026-03-04FDA-DeviceEdermyClass IINationwideStop using Edermy PIE PAK devices
Lack of 510K clearance
- 2026-03-04FDA-DeviceEdermyClass IINationwideStop using Edermy PIE Trolley System Model 2005
Lack of 510K clearance
- 2026-03-04FDA-DeviceEncore MedicalClass IINationwideCheck your Encore Medical shoulder implant labeling
Knee and Humeral socket implants contain incorrect labeling.
- 2026-03-04FDA-DeviceEncore MedicalClass IINationwideCheck Encore Medical knee implant labeling
Knee and Humeral socket implants contain incorrect labeling.
- 2026-03-04FDA-DeviceEncore MedicalClass IINationwideCheck reverse shoulder implant labeling
Knee and Humeral socket implants contain incorrect labeling.
- 2026-03-04FDA-DeviceOlympusClass IINationwideStop using Olympus Resection Sheath A2666T
Complaints of the ceramic tip of the resection sheath breaking have been received.
- 2026-03-04FDA-DeviceOlympusClass IINationwideStop using Olympus Inner Sheath Model A2642
Complaints of the ceramic tip of the resection sheath breaking have been received.
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