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. 2,679 recalls have been distributed to Pennsylvania in the last 12 months.

55,602 total recalls
2,679 in last 12 months

Showing 2890128920 of 29,947 recalls

Medical DeviceAugust 17, 2012· Varian Medical Systems, Inc. Oncology Systems

Recalled Item: Varian brand Eclipse Treatment Planning System Recalled by Varian Medical...

The Issue: Varian has identified an anomaly with the Eclipse Treatment Planning where...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 17, 2012· Stryker Howmedica Osteonics Corp.

Recalled Item: Stryker Orthopaedics Torx 6.5mm Cancellous Bone Screw The Recalled by...

The Issue: Stryker has received reports from the field indicating that certain lots of...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2012· Karl Storz Endoscopy America Inc

Recalled Item: KARL STORZ Photodynamic Diagnosis (PDD) D-Light C System Recalled by Karl...

The Issue: The recall was initiated because Karl Storz has confirmed that the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2012· GE Healthcare, LLC

Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare has...

The Issue: GE Healthcare has recently become aware of a potential safety issue with...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2012· ZOLL Medical Corporation

Recalled Item: Zoll X Series Defibrillator/Pacemaker/Monitor Product Usage: The product is...

The Issue: Shipped with incorrect software

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2012· Surgical Specialties Puerto Rico Inc. dba Angiotech PR Inc.

Recalled Item: "***Sharpoint IQ Geometry Slit Knife Angled Recalled by Surgical Specialties...

The Issue: Potential for bent tips.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2012· Philips Healthcare Inc.

Recalled Item: Philips SureSigns VSi/VS2+ patient monitors Model Part Numbers VSi/ 863275...

The Issue: Philips SureSigns VSi/VS2+ patient monitors may not be properly secured and...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2012· Surgical Specialties Puerto Rico Inc. dba Angiotech PR Inc.

Recalled Item: "***Sharpoint IQ Geometry Slit Knife Angled Recalled by Surgical Specialties...

The Issue: Potential for bent tips.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2012· Surgical Specialties Puerto Rico Inc. dba Angiotech PR Inc.

Recalled Item: "***Sharpoint IQ Geometry Slit Knife Angled Recalled by Surgical Specialties...

The Issue: Potential for bent tips.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2012· Surgical Specialties Puerto Rico Inc. dba Angiotech PR Inc.

Recalled Item: "***Sharpoint IQ Geometry Slit Knife Angled Recalled by Surgical Specialties...

The Issue: Potential for bent tips.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2012· Sorin Group USA, Inc.

Recalled Item: Stockert Heater-Cooler 3T Recalled by Sorin Group USA, Inc. Due to On August...

The Issue: On August 15, 2012, Sorin informed consignees via letter of changes made to...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 14, 2012· Biomet, Inc.

Recalled Item: JUGGERKNOT IN¿GUIDE PUNCH Recalled by Biomet, Inc. Due to Investigation...

The Issue: Investigation found that the current design of the product allows the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 14, 2012· Lansinoh Laboratories Inc

Recalled Item: THERA PEARL 3-in-1 BREAST THERAPY Recalled by Lansinoh Laboratories Inc Due...

The Issue: The Spanish translation on the Instructions for Use (IFU) insert and product...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2012· Mindray DS USA, Inc. d.b.a. Mindray North America

Recalled Item: Mindray A3 Anesthesia Delivery System Manufactured in China for Mindray...

The Issue: Mindray has identified the potential for a system leak resulting an issue...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 13, 2012· Vital Images, Inc.

Recalled Item: Software for Vitrea Recalled by Vital Images, Inc. Due to Vital Images has...

The Issue: Vital Images has found two potential errors in calcium score values in...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2012· GE Healthcare, LLC

Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare became...

The Issue: GE Healthcare became aware of a potential issue related to incorrect image...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2012· Mindray DS USA, Inc. d.b.a. Mindray North America

Recalled Item: Mindray A5 Anesthesia Delivery System Manufactured in China for Mindray...

The Issue: Mindray has identified the potential for a system leak resulting an issue...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 13, 2012· Neomend Inc

Recalled Item: Progel Pleural Air Leak Sealant Recalled by Neomend Inc Due to Product was...

The Issue: Product was distributed with an incorrect expiration date. Product was...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2012· Immunodiagnostics Systems Ltd

Recalled Item: IDS Urine BETA CrossLaps ELISA Recalled by Immunodiagnostics Systems Ltd Due...

The Issue: It has been noted by staff at IDS Inc. that stock of the affected products...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2012· Immunodiagnostics Systems Ltd

Recalled Item: IDS-iSYS Intact PINP Control Set Recalled by Immunodiagnostics Systems Ltd...

The Issue: It has been noted by staff at IDS Inc. that stock of the affected products...

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

Class II — Potential Health HazardOngoing