Pennsylvania recalls
3,594 federal recalls affecting Pennsylvania in the last 12 months - 382 Pennsylvania-specific plus 3,212 nationwide. Sourced from CPSC, FDA, USDA, and NHTSA.
- 2026-06-24FDA-DeviceMedlineClass IINationwideMedline medical procedure kits recalled for catheter defects
During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surface finish, instances where the catheter connector detached prematurely from the catheter funnel, and limited cases where the catheter outer diameter did not meet specification.
- 2026-06-24FDA-DeviceMedlineClass IINationwideMedline gynecological kits recalled for catheter defects
During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surface finish, instances where the catheter connector detached prematurely from the catheter funnel, and limited cases where the catheter outer diameter did not meet specification.
- 2026-06-24FDA-DeviceMedlineClass IINationwideMedline Pelvic Lap Pack recalled for catheter defects
During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surface finish, instances where the catheter connector detached prematurely from the catheter funnel, and limited cases where the catheter outer diameter did not meet specification.
- 2026-06-24FDA-DeviceMedlineClass IINationwideMedline procedure kits recalled for catheter defects
During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surface finish, instances where the catheter connector detached prematurely from the catheter funnel, and limited cases where the catheter outer diameter did not meet specification.
- 2026-06-24FDA-DeviceMedlineClass IINationwideMedline procedure kits recalled for catheter defects
During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surface finish, instances where the catheter connector detached prematurely from the catheter funnel, and limited cases where the catheter outer diameter did not meet specification.
- 2026-06-24FDA-DeviceMedlineClass IINationwideMedline Nursing Kit recalled for catheter defects
During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surface finish, instances where the catheter connector detached prematurely from the catheter funnel, and limited cases where the catheter outer diameter did not meet specification.
- 2026-06-24FDA-DeviceMedlineClass IINationwideMedline DR FERNANDEZ kit recalled for catheter defects
During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surface finish, instances where the catheter connector detached prematurely from the catheter funnel, and limited cases where the catheter outer diameter did not meet specification.
- 2026-06-24FDA-DeviceMedlineClass IINationwideMedline procedure kits recalled for catheter defects
During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surface finish, instances where the catheter connector detached prematurely from the catheter funnel, and limited cases where the catheter outer diameter did not meet specification.
- 2026-06-24FDA-DeviceMedlineClass IINationwideMedline procedure kits recalled for catheter connector detachment
During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surface finish, instances where the catheter connector detached prematurely from the catheter funnel, and limited cases where the catheter outer diameter did not meet specification.
- 2026-06-24FDA-DeviceMedlineClass IINationwideMedline urethroplasty kits recalled for catheter defects
During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surface finish, instances where the catheter connector detached prematurely from the catheter funnel, and limited cases where the catheter outer diameter did not meet specification.
- 2026-06-24FDA-DeviceMedlineClass IINationwideMedline Tonsil Pack Cath kits recalled for catheter defects
During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surface finish, instances where the catheter connector detached prematurely from the catheter funnel, and limited cases where the catheter outer diameter did not meet specification.
- 2026-06-24FDA-DeviceMedlineClass IINationwideMedline procedure kits recalled for catheter defects
During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surface finish, instances where the catheter connector detached prematurely from the catheter funnel, and limited cases where the catheter outer diameter did not meet specification.
- 2026-06-24FDA-DeviceMedlineClass IINationwideMedline Robinson catheters recalled for connector detachment risk
During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surface finish, instances where the catheter connector detached prematurely from the catheter funnel, and limited cases where the catheter outer diameter did not meet specification.
- 2026-06-24FDA-DeviceMedlineClass IINationwideMedline procedure kits recalled for catheter defects
During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surface finish, instances where the catheter connector detached prematurely from the catheter funnel, and limited cases where the catheter outer diameter did not meet specification.
- 2026-06-24FDA-DeviceMedlineClass IINationwideMedline Oral Restoration Kit recalled for catheter defects
During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surface finish, instances where the catheter connector detached prematurely from the catheter funnel, and limited cases where the catheter outer diameter did not meet specification.
- 2026-06-24FDA-DeviceMedlineClass IINationwideMedline vasectomy reversal kit recalled for catheter defects
During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surface finish, instances where the catheter connector detached prematurely from the catheter funnel, and limited cases where the catheter outer diameter did not meet specification.
- 2026-06-24FDA-DeviceMedlineClass IINationwideMedline procedure kits recalled for catheter defects
During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surface finish, instances where the catheter connector detached prematurely from the catheter funnel, and limited cases where the catheter outer diameter did not meet specification.
- 2026-06-24FDA-DeviceMedlineClass IINationwideMedline cardiac procedure kits recalled for catheter defects
During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surface finish, instances where the catheter connector detached prematurely from the catheter funnel, and limited cases where the catheter outer diameter did not meet specification.
- 2026-06-24FDA-DeviceMedlineClass IINationwideMedline cardiac procedure kits recalled for catheter defects
During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surface finish, instances where the catheter connector detached prematurely from the catheter funnel, and limited cases where the catheter outer diameter did not meet specification.
- 2026-06-24FDA-DeviceMedlineClass IINationwideMedline laparoscopy kits recalled for catheter defects
During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surface finish, instances where the catheter connector detached prematurely from the catheter funnel, and limited cases where the catheter outer diameter did not meet specification.
- 2026-06-24FDA-DeviceMedlineClass IINationwideMedline latex catheter recalled for connector detachment risk
During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surface finish, instances where the catheter connector detached prematurely from the catheter funnel, and limited cases where the catheter outer diameter did not meet specification.
- 2026-06-24FDA-DeviceMedlineClass IINationwideMedline latex catheter recalled for connector detachment risk
During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surface finish, instances where the catheter connector detached prematurely from the catheter funnel, and limited cases where the catheter outer diameter did not meet specification.
- 2026-06-24FDA-DeviceMedlineClass IINationwideMedline urethral catheter trays recalled for connector detachment risk
During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surface finish, instances where the catheter connector detached prematurely from the catheter funnel, and limited cases where the catheter outer diameter did not meet specification.
- 2026-06-24FDA-DeviceMedlineClass IINationwideMedline urethral catheter tray recalled for connector detachment risk
During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surface finish, instances where the catheter connector detached prematurely from the catheter funnel, and limited cases where the catheter outer diameter did not meet specification.
- 2026-06-24FDA-DeviceMedlineClass IINationwideMedline urethral catheterization trays recalled for defects
During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surface finish, instances where the catheter connector detached prematurely from the catheter funnel, and limited cases where the catheter outer diameter did not meet specification.
- 2026-06-24FDA-DeviceMedlineClass IINationwideMedline urethral catheters recalled for connector detachment risk
During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surface finish, instances where the catheter connector detached prematurely from the catheter funnel, and limited cases where the catheter outer diameter did not meet specification.
- 2026-06-24FDA-DeviceMito Red LightClass IINationwideMito Red Light Super Mobile recalled for battery fire risk
The near-infrared therapy device contains a lithium-ion battery that may malfunction, causing it to catch fire or burst into flames.
- 2026-06-24FDA-DeviceGEClass IINationwideGE Giraffe OmniBed recalled for loose fastener risk
GE HealthCare has become aware of a potential issue involving the canopy soffit beneath the control panel end of the device. Under certain conditions, for example, impact during transport, one or more of the fasteners that secure the soffit can disengage. If this occurs, a fastener could fall into the patient compartment. In rare circumstances, if multiple fasteners disengage, the canopy soffit can become loose or detach. These conditions could potentially result in patient injury.
- 2026-06-24FDA-DeviceGEClass IINationwideGE Giraffe OmniBed Carestation recalled for fastener hazard
GE HealthCare has become aware of a potential issue involving the canopy soffit beneath the control panel end of the device. Under certain conditions, for example, impact during transport, one or more of the fasteners that secure the soffit can disengage. If this occurs, a fastener could fall into the patient compartment. In rare circumstances, if multiple fasteners disengage, the canopy soffit can become loose or detach. These conditions could potentially result in patient injury.
- 2026-06-24FDA-DeviceGEClass IINationwideGE Giraffe OmniBed recalled for loose fastener risk
GE HealthCare has become aware of a potential issue involving the canopy soffit beneath the control panel end of the device. Under certain conditions, for example, impact during transport, one or more of the fasteners that secure the soffit can disengage. If this occurs, a fastener could fall into the patient compartment. In rare circumstances, if multiple fasteners disengage, the canopy soffit can become loose or detach. These conditions could potentially result in patient injury.
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