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. 2,885 recalls have been distributed to Pennsylvania in the last 12 months.
Showing 5041–5060 of 29,947 recalls
Recalled Item: Cardinal Health Monoject Recalled by Cardinal Health 200, LLC Due to...
The Issue: Cardinal Health is expanding their previous product correction actions to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardinal Health Monoject Recalled by Cardinal Health 200, LLC Due to The...
The Issue: The listed lots of Cardinal Health Monoject Enteral Syringes with ENFit (6,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bubble Sensor (.5720) Recalled by Maquet Medical Systems USA Due to The...
The Issue: The Bubble Sensor optional accessory to the CARDIOHELP-i extracorporeal life...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardinal Health Monoject Recalled by Cardinal Health 200, LLC Due to...
The Issue: Cardinal Health is expanding their previous product correction actions to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardinal Health Monoject Recalled by Cardinal Health 200, LLC Due to...
The Issue: Cardinal Health is expanding their previous product correction actions to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardinal Health Monoject Recalled by Cardinal Health 200, LLC Due to The...
The Issue: The listed lots of Cardinal Health Monoject Enteral Syringes with ENFit (6,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardinal Health Monoject Recalled by Cardinal Health 200, LLC Due to...
The Issue: Cardinal Health is expanding their previous product correction actions to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardinal Health Monoject Recalled by Cardinal Health 200, LLC Due to The...
The Issue: The listed lots of Cardinal Health Monoject Enteral Syringes with ENFit (6,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardinal Health Monoject Recalled by Cardinal Health 200, LLC Due to...
The Issue: Cardinal Health is expanding their previous product correction actions to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardinal Health Monoject Recalled by Cardinal Health 200, LLC Due to...
The Issue: Cardinal Health is expanding their previous product correction actions to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardinal Health Monoject Recalled by Cardinal Health 200, LLC Due to...
The Issue: Cardinal Health is expanding their previous product correction actions to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Impella catheters - Intravascular micro axial blood pumps that support...
The Issue: New warnings are being added to the Instructions for Use for all affected...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Impella catheters - Intravascular micro axial blood pumps that support...
The Issue: IFU has been updated to include warnings about the risk of the inlet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Senographe Pristina Recalled by GE Medical Systems, SCS Due to X-ray...
The Issue: X-ray exposure termination audible signal on Senographe Pristina with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Power Knee Recalled by Ossur H / F Due to Knee batteries may need...
The Issue: Knee batteries may need replacement with conforming batteries to ensure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ELEOS COLLAR STEM Recalled by Onkos Surgical, Inc. Due to Mislabeling
The Issue: Mislabeling of 13mm Modular Segmental Stem package (HC-13120-03M) which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ELEOS COLLAR STEM Recalled by Onkos Surgical, Inc. Due to Mislabeling
The Issue: Mislabeling of 13mm Modular Segmental Stem package (HC-13120-03M) which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HRIS ACET CUP CUT TIP 26X140 Part Number: 6210-5-100. single-use Recalled by...
The Issue: Failed to meet the acceptance criteria for the seal integrity and/or package...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HRIS ACET CUP CUT TIP 32X140 Part Number: 6210-5-200rker. single-use...
The Issue: Failed to meet the acceptance criteria for the seal integrity and/or package...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PATTERSON¿ PROCEDURE EARLOOP MASKS- ANTI-FOG Recalled by AMD Medicom Inc....
The Issue: Level 3 masks were produced on alternate non-validated production equipment...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.