Product Recalls in Pennsylvania

Product recalls affecting Pennsylvania — including food, drugs, consumer products, medical devices, and vehicles distributed to Pennsylvania. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,924 recalls have been distributed to Pennsylvania in the last 12 months.

55,602 total recalls
2,924 in last 12 months

Showing 281300 of 55,602 recalls

Medical DeviceJanuary 7, 2026· Medline Industries, LP

Recalled Item: Medline Convenience Kits: 1) KIT GENERAL CLOSURE Recalled by Medline...

The Issue: Medline has identified issues related to calibration of the equipment used...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2026· Medline Industries, LP

Recalled Item: Medline Convenience Kits: 1) LVAD DRIVELINE TRAY Recalled by Medline...

The Issue: Medline has identified issues related to calibration of the equipment used...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2026· Medline Industries, LP

Recalled Item: Medline Convenience Kits: 1) OR ARTERIOGRAM Recalled by Medline Industries,...

The Issue: Medline has identified issues related to calibration of the equipment used...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2026· Medline Industries, LP

Recalled Item: Medline Convenience Kits: 1) KIT TRIPLE LUMEN INSERTION Recalled by Medline...

The Issue: Medline has identified issues related to calibration of the equipment used...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2026· Medline Industries, LP

Recalled Item: Medline Convenience Kits: 1) LITHOTOMY PACK Recalled by Medline Industries,...

The Issue: Medline has identified issues related to calibration of the equipment used...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2026· Medline Industries, LP

Recalled Item: Medline Convenience Kits: 1) DRAPE PACK-CHOICE Recalled by Medline...

The Issue: Medline has identified issues related to calibration of the equipment used...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2026· Medline Industries, LP

Recalled Item: Medline Convenience Kits: 1) WMC I D PACK-LF Recalled by Medline Industries,...

The Issue: Medline has identified issues related to calibration of the equipment used...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2026· Medline Industries, LP

Recalled Item: Medline Convenience Kits: 1) ENDO KIT W/SYRINGE Recalled by Medline...

The Issue: Medline has identified issues related to calibration of the equipment used...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2026· Medline Industries, LP

Recalled Item: Medline Convenience Kits: 1) C-SECTION PACK Recalled by Medline Industries,...

The Issue: Medline has identified issues related to calibration of the equipment used...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2026· Medline Industries, LP

Recalled Item: Medline Convenience Kits: 1) DRAPE PACK Recalled by Medline Industries, LP...

The Issue: Medline has identified issues related to calibration of the equipment used...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 6, 2026· VANTIVE US HEALTHCARE LLC

Recalled Item: PRISMAFLEX HF1000 SET Recalled by VANTIVE US HEALTHCARE LLC Due to There is...

The Issue: There is a potential dislodgement of the Prismaflex Set deaeration chamber...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 6, 2026· VANTIVE US HEALTHCARE LLC

Recalled Item: PRISMAFLEX TPE2000 SET Recalled by VANTIVE US HEALTHCARE LLC Due to There is...

The Issue: There is a potential dislodgement of the Prismaflex Set deaeration chamber...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 6, 2026· VANTIVE US HEALTHCARE LLC

Recalled Item: PRISMAFLEX M150 SET Recalled by VANTIVE US HEALTHCARE LLC Due to There is a...

The Issue: There is a potential dislodgement of the Prismaflex Set deaeration chamber...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 6, 2026· VANTIVE US HEALTHCARE LLC

Recalled Item: PRISMAFLEX HF1000 SET Recalled by VANTIVE US HEALTHCARE LLC Due to There is...

The Issue: There is a potential dislodgement of the Prismaflex Set deaeration chamber...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 6, 2026· VANTIVE US HEALTHCARE LLC

Recalled Item: OXIRIS SET Recalled by VANTIVE US HEALTHCARE LLC Due to There is a potential...

The Issue: There is a potential dislodgement of the Prismaflex Set deaeration chamber...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
FoodJanuary 6, 2026· Herbs Forever

Recalled Item: HerbsForever- Hingwastika Churna Recalled by Herbs Forever Due to Undeclared...

The Issue: Potential undeclared allergen ingredient (Wheat)

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJanuary 6, 2026· VANTIVE US HEALTHCARE LLC

Recalled Item: PRIMSAFLEX M100 SET Recalled by VANTIVE US HEALTHCARE LLC Due to There is a...

The Issue: There is a potential dislodgement of the Prismaflex Set deaeration chamber...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
FoodJanuary 6, 2026· Herbs Forever

Recalled Item: HerbsForever- Gastro Care Recalled by Herbs Forever Due to Undeclared Allergen

The Issue: Potential undeclared allergen ingredient (Wheat)

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 6, 2026· Encon Safety Products Co

Recalled Item: AQ 120 GFEW Recalled by Encon Safety Products Co Due to cGMP deviations.

The Issue: cGMP deviations.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 6, 2026· Straumann USA LLC

Recalled Item: WB Impression Post Closed Tray incl. guide screw Recalled by Straumann USA...

The Issue: The mix up of the impression caps provided in the package. The provided...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing