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. 2,691 recalls have been distributed to Pennsylvania in the last 12 months.

55,602 total recalls
2,691 in last 12 months

Showing 2406124080 of 29,947 recalls

Medical DeviceJanuary 13, 2015· Sony Medical Systems

Recalled Item: Sony LMD-1951MD Recalled by Sony Medical Systems Due to Tthe medical monitor...

The Issue: Tthe medical monitor has either not turned on or has lost image during...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 13, 2015· GE Inspection Technologies, LP

Recalled Item: GE Inspection Technologies x|tome|x L240 an Cabinet X-ray system Recalled by...

The Issue: It was discovered that the upper left corner-shaped lead shield in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 13, 2015· Siemens Medical Solutions USA, Inc

Recalled Item: Syngo.plaza: Syngo.plaza is a Picture Archiving and Communication System...

The Issue: In case of a system crash, images may not be written to the hard disk and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 13, 2015· Teleflex Medical

Recalled Item: LMA (Laryngeal Mask Airway) Supreme (New Cuff) Size 5 Recalled by Teleflex...

The Issue: The labelling of units from the affected lot indicates that it contains a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 13, 2015· Medtronic Sofamor Danek USA Inc

Recalled Item: KYPHON EXPRESS Recalled by Medtronic Sofamor Danek USA Inc Due to The...

The Issue: The product, labeled as containing, one bevel-tipped instrument and one...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 13, 2015· CareFusion 303, Inc.

Recalled Item: SmartSite Low Sorbing Infusion Set Recalled by CareFusion 303, Inc. Due to...

The Issue: CareFusion is recalling the SmartSite Low Sorbing Infusion set due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 12, 2015· Maquet Cardiovascular Us Sales, Llc

Recalled Item: Servo-I ventilator system CO2 analyzer. Part number 65 23 588. Recalled by...

The Issue: A calibration problem was detected in a specific number of the Servo-I...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 12, 2015· Covidien LP (formerly Nellcor Puritan Bennett Inc.)

Recalled Item: Puritan Bennett 980 Ventilator System Recalled by Covidien LP (formerly...

The Issue: Covidien is issuing a voluntary field action for all Puritan Bennett 980...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2015· Navilyst Medical, Inc

Recalled Item: NAMIC Convenience Kit Recalled by Navilyst Medical, Inc Due to The labelled...

The Issue: The labelled expiration dating of the affected product is not fully...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2015· Navilyst Medical, Inc

Recalled Item: NAMIC Convenience Kit Recalled by Navilyst Medical, Inc Due to The labelled...

The Issue: The labelled expiration dating of the affected product is not fully...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2015· Navilyst Medical, Inc

Recalled Item: NAMIC Convenience Kit Recalled by Navilyst Medical, Inc Due to The labelled...

The Issue: The labelled expiration dating of the affected product is not fully...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2015· Navilyst Medical, Inc

Recalled Item: NAMIC Convenience Kit Recalled by Navilyst Medical, Inc Due to The labelled...

The Issue: The labelled expiration dating of the affected product is not fully...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2015· Navilyst Medical, Inc

Recalled Item: NAMIC Convenience Kit Recalled by Navilyst Medical, Inc Due to The labelled...

The Issue: The labelled expiration dating of the affected product is not fully...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2015· Navilyst Medical, Inc

Recalled Item: NAMIC Convenience Kit Recalled by Navilyst Medical, Inc Due to The labelled...

The Issue: The labelled expiration dating of the affected product is not fully...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2015· Navilyst Medical, Inc

Recalled Item: NAMIC Convenience Kit Recalled by Navilyst Medical, Inc Due to The labelled...

The Issue: The labelled expiration dating of the affected product is not fully...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2015· Arrow International Inc

Recalled Item: Arrow Select Kits (ASK) Recalled by Arrow International Inc Due to Certain...

The Issue: Certain product codes and lot numbers of Kits with Biopatch Dressing were...

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

Class III — Low RiskOngoing
Medical DeviceJanuary 9, 2015· Navilyst Medical, Inc

Recalled Item: NAMIC Convenience Kit Recalled by Navilyst Medical, Inc Due to The labelled...

The Issue: The labelled expiration dating of the affected product is not fully...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2015· Medtronic Neuromodulation

Recalled Item: The Medtronic Recalled by Medtronic Neuromodulation Due to Current labeling...

The Issue: Current labeling indicates that cycling improves device longevity in every...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2015· Navilyst Medical, Inc

Recalled Item: NAMIC Convenience Kit Recalled by Navilyst Medical, Inc Due to The labelled...

The Issue: The labelled expiration dating of the affected product is not fully...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2015· Navilyst Medical, Inc

Recalled Item: NAMIC Convenience Kit Recalled by Navilyst Medical, Inc Due to The labelled...

The Issue: The labelled expiration dating of the affected product is not fully...

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

Class II — Potential Health HazardOngoing