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. 1,042 recalls have been distributed to Pennsylvania in the last 12 months.
Showing 25141–25160 of 55,602 recalls
Recalled Item: Prometra II Programmable Pump Recalled by Flowonix Medical Inc Due to The...
The Issue: The pump shuts down unexpectedly if Error 115, an alarm associated with a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: syngo.via syngo.CT Cardiac Planning Recalled by Siemens Medical Solutions...
The Issue: There is a potential risk of a wrong measurement in the annulus plane during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EV1000 Clinical Platform Recalled by Edwards Lifesciences, LLC Due to...
The Issue: Potential for an electrical short circuit leading to possible fire hazard...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prometra II Programmable Pump (Clinical) Recalled by Flowonix Medical Inc...
The Issue: The pump shuts down unexpectedly if Error 115, an alarm associated with a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rifton E-Pacer Recalled by Community Products, LLC Due to A design change to...
The Issue: A design change to the load-bearing quick release buckle renders the springs...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Better Made Snack Foods Family Size $3.99 Original Potato Chips Recalled by...
The Issue: Undeclared milk
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Siemens Digital Linear Accelerators of type: ARTISTE MV System MEVATRON...
The Issue: Advisory issued not to disable or bypass the AMP function. Disabling or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet Servo-I Ventilator System -EDI CATHETER PHT Free 6Fr/49cm 5/pkg...
The Issue: Edi Catheter labeled with wrong expiry date on single pack EDI catheter boxes
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS XT 7600 Integrated System Recalled by Ortho-Clinical Diagnostics Due...
The Issue: Potential for sample fluid to be dispensed to an incorrect position on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AIR Technology Anterior Array Recalled by GE Healthcare, LLC Due to The...
The Issue: The outer seam of the coil, closest to the system cable, may separate and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OnSight 3D Extremity System- X-Ray Recalled by Carestream Health, Inc. Due...
The Issue: When the user performs the re-assignment of a parent / companion pair, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOPHEN UFH Control C1 Recalled by Aniara Diagnostica LLC Due to The...
The Issue: The manufacturer packaged incorrect versions of the Instructions for Use...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Performance Series Sagittal Blade Recalled by Stryker Instruments Div. of...
The Issue: During manufacture, packaging materials for a small portion of the lot may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Neomem Resorbable Collagen Membrane Recalled by Collagen Matrix, Inc. Due to...
The Issue: Product was packaged in the wrong box; may have been placed inside a Neomem...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOPHEN UFH Control C2 Recalled by Aniara Diagnostica LLC Due to The...
The Issue: The manufacturer packaged incorrect versions of the Instructions for Use...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOPHEN LMWH Control C4 Recalled by Aniara Diagnostica LLC Due to The...
The Issue: The manufacturer packaged incorrect versions of the Instructions for Use...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Walgreens Probiotic 12.5 Billion Active Cultures Recalled by Merical, LLC...
The Issue: Incorrect probiotic strain used in formulation which did not match product...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Gavilyte-N Recalled by LUPIN SOMERSET Due to Labeling Not Elsewhere...
The Issue: Labeling Not Elsewhere Classified; orange and cherry flavor packets...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Diclofenac Sodium Topical Solution Recalled by Ingenus Pharmaceuticals Llc...
The Issue: Defective Container: firm discovered samples stored horizontally as well as...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cios Alpha Recalled by Siemens Medical Solutions USA, Inc Due to Continuous...
The Issue: Continuous operation at very high tube output may result in increased wear...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.