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. 1,041 recalls have been distributed to Pennsylvania in the last 12 months.

55,602 total recalls
1,041 in last 12 months

Showing 28501–28520 of 55,602 recalls

Medical DeviceMay 11, 2018· Smith & Nephew, Inc.

Recalled Item: Birmingham Hip Resurfacing Acetabular Cup with Impactor: (a) Size 56 mm...

The Issue: The affected devices are manufactured to the same design specification as...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2018· Olympus Corporation of the Americas

Recalled Item: Olympus JF-140F duodenoscopes (Model NumberJF-140F) Recalled by Olympus...

The Issue: Issuance of validated, new reprocessing procedures. This corrective action...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2018· Olympus Corporation of the Americas

Recalled Item: Olympus JF-160F duodenoscopes (Model NumberJF-160F) Recalled by Olympus...

The Issue: Issuance of validated, new reprocessing procedures. The new cleaning...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2018· Smith & Nephew, Inc.

Recalled Item: Birmingham Hip Resurfacing Femoral Head: (a) Size 58 mm Recalled by Smith &...

The Issue: The affected devices are manufactured to the same design specification as...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2018· Zimmer Biomet, Inc.

Recalled Item: Vanguard Knee System PS Tibial Bearing Recalled by Zimmer Biomet, Inc. Due...

The Issue: The label master file was errantly set up as a 63/37mm instead of a 63/67mm....

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

Class II — Potential Health HazardOngoing
DrugMay 11, 2018· L. Perrigo Company

Recalled Item: Scopolamine Transdermal Therapeutic System Recalled by L. Perrigo Company...

The Issue: Defective delivery system

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 10, 2018· Zimmer Dental Inc

Recalled Item: Outer Package Label: Tapered Screw-Vent Implant System Recalled by Zimmer...

The Issue: Dental implants have incorrect item/lot numbers and size on the inner...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2018· Mako Surgical Corporation

Recalled Item: Rio System Irrigation Clip - Catalog # 111690 Product Usage: Recalled by...

The Issue: Out of tolerance.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2018· FHC, Inc.

Recalled Item: microTargeting" Drive System Recalled by FHC, Inc. Due to The FHC Depth Stop...

The Issue: The FHC Depth Stop Adapter may cause damage to the lead and stylet when the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2018· Angiodynamics Inc. (Navilyst Medical Inc.)

Recalled Item: RS 5F DL BIOFLO PICC Recalled by Angiodynamics Inc. (Navilyst Medical Inc.)...

The Issue: A component of the kits might contain unsafe levels of bacterial endotoxins...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2018· Angiodynamics Inc. (Navilyst Medical Inc.)

Recalled Item: RS 5F DL BIOFLO PASV Recalled by Angiodynamics Inc. (Navilyst Medical Inc.)...

The Issue: A component of the kits might contain unsafe levels of bacterial endotoxins...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2018· Angiodynamics Inc. (Navilyst Medical Inc.)

Recalled Item: RS TANDEM 5F DL XCELA PICC PASV Recalled by Angiodynamics Inc. (Navilyst...

The Issue: A component of the kits might contain unsafe levels of bacterial endotoxins...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2018· Angiodynamics Inc. (Navilyst Medical Inc.)

Recalled Item: Bio-Stable 5F DL-55CM IR-145 Kit Non-Valved PG Recalled by Angiodynamics...

The Issue: A component of the kits might contain unsafe levels of bacterial endotoxins...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2018· Angiodynamics Inc. (Navilyst Medical Inc.)

Recalled Item: BioFlo PICC (Valved) 5FDL-55cm Maximal Barrier Nursing Kit w/70cm Nitinol...

The Issue: A component of the kits might contain unsafe levels of bacterial endotoxins...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2018· Angiodynamics Inc. (Navilyst Medical Inc.)

Recalled Item: RS 5F DL BIOFLO PASV Recalled by Angiodynamics Inc. (Navilyst Medical Inc.)...

The Issue: A component of the kits might contain unsafe levels of bacterial endotoxins...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2018· Angiodynamics Inc. (Navilyst Medical Inc.)

Recalled Item: Xcela 5FDL-55cm Maximal Barrier Nursing Kit PG Recalled by Angiodynamics...

The Issue: A component of the kits might contain unsafe levels of bacterial endotoxins...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2018· Life Technologies, Corp.

Recalled Item: Gibco RPMI 1640 Medium Recalled by Life Technologies, Corp. Due to It has...

The Issue: It has been determined that the fill port tube seal integrity was...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2018· Angiodynamics Inc. (Navilyst Medical Inc.)

Recalled Item: TANDEM 5F DL BIOFLO PASV Recalled by Angiodynamics Inc. (Navilyst Medical...

The Issue: A component of the kits might contain unsafe levels of bacterial endotoxins...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2018· Angiodynamics Inc. (Navilyst Medical Inc.)

Recalled Item: RS 5F DL XCELA PICC Recalled by Angiodynamics Inc. (Navilyst Medical Inc.)...

The Issue: A component of the kits might contain unsafe levels of bacterial endotoxins...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2018· Angiodynamics Inc. (Navilyst Medical Inc.)

Recalled Item: 5F DL BIOFLO PASV Recalled by Angiodynamics Inc. (Navilyst Medical Inc.) Due...

The Issue: A component of the kits might contain unsafe levels of bacterial endotoxins...

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

Class II — Potential Health HazardOngoing