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. 2,708 recalls have been distributed to Pennsylvania in the last 12 months.
Showing 21301–21320 of 29,947 recalls
Recalled Item: SOMATOM Force Recalled by Siemens Medical Solutions USA, Inc Due to The...
The Issue: The Neonate Head protocol with the pediatric kernel Hp38 could result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity Core-Computed Tomography X-ray system Product Usage: The Ingenuity...
The Issue: Philips Healthcare received reports from the field that certain Ingenuity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dialog+ Hemodialysis machines: Dialog + 120 V DF+Adimea+WAN-BSL Product Code...
The Issue: Potential leakage of conductivity sensors of the Dialog Dialysis machines.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity Core 128-Computed Tomography X-ray system Product Usage: The...
The Issue: Philips Healthcare received reports from the field that certain Ingenuity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance 64 Recalled by Philips Medical Systems (Cleveland) Inc Due to...
The Issue: Philips Healthcare received reports from the field that certain Brilliance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Various trauma and sports medicine instruments and implants. Arthroscope....
The Issue: Insufficient seal strength on sterile barrier packaging. The seal could be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dialog+ Hemodialysis machines: Conductivity Sensor (BIC) Item # 3456102A The...
The Issue: Potential leakage of conductivity sensors of the Dialog Dialysis machines.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Various trauma and sports medicine instruments and implants. Orthopedic...
The Issue: Insufficient seal strength on sterile barrier packaging. The seal could be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dialog+ Hemodialysis machines: Dialog A + HE/BIC Product Code 710200L...
The Issue: Potential leakage of conductivity sensors of the Dialog Dialysis machines.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: American Surgical Americot Blue 3/8" x 3/4" : 20-14S Recalled by American...
The Issue: Product packaging defective compromising sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: American Surgical Delicot 5 mm x 8 mm : Recalled by American Surgical...
The Issue: Product packaging defective compromising sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: American Surgical Delicot-J 30 mm x 70 mm : Recalled by American Surgical...
The Issue: Product packaging defective compromising sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mach 4 Mouse Probe vial within the Mach 4 Universal HRP-Polymer Kit Recalled...
The Issue: Biocare Medical has identified a single lot (082715) of its Mach 4 HRP...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: X-Ray Diagnostic Table Recalled by Shimadzu Medical Systems Due to Report of...
The Issue: Report of unintentional movement of table to reverse tilting.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Trucount Absolute Counting Tubes: Model number: 340334 IVD Recalled by...
The Issue: One lot of lot of BD Trucount tubes may contain tubes from another lot....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hologic InPlex CF Molecular Test (IVD) Recalled by Hologic, Inc Due to...
The Issue: Complaints of false positive HET mutations and leaking cards; could lead to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CF InPlex ASR Card Recalled by Hologic, Inc Due to Complaints of false...
The Issue: Complaints of false positive HET mutations and leaking cards; could lead to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ellipse ICD (Implantable Cardioverter Defibrillator) Model CD2411-36Q...
The Issue: St. Jude Medical is recalling the Ellipse ICD (Implantable Cardioverter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mass Eye & Ear Finger Cot Nasal 2's : Recalled by American Surgical Company...
The Issue: Product packaging defective compromising sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: American Surgical Tonsil Sponges 1" Large : 50-01 Product Recalled by...
The Issue: Product packaging defective compromising sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.