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. 2,078 recalls have been distributed to Pennsylvania in the last 12 months.

55,602 total recalls
2,078 in last 12 months

Showing 1308113100 of 29,947 recalls

Medical DeviceOctober 25, 2019· Conformis, Inc.

Recalled Item: iTotal CR Knee Replacement System Model Number: TCR-111-1111-010102 -...

The Issue: Medial and lateral polyethylene inserts did not securely fit into the cobalt...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2019· Boston Scientific Corporation

Recalled Item: Rebel Monorail PtCr Coronary Stent System Recalled by Boston Scientific...

The Issue: Certain dilation and extension catheters are being recalled because these...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2019· Centurion Medical Products Corporation

Recalled Item: Centurion Medical Products UNIVERSAL LINE FULL BODY DRAPE KIT - Recalled by...

The Issue: Sterile packaging incomplete seals may compromise sterility of the product

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2019· Boston Scientific Corporation

Recalled Item: NC Emerge Monorail PTCA Dilatation Catheter. Sterilized using ethylene...

The Issue: Certain dilation and extension catheters are being recalled because these...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2019· Boston Scientific Corporation

Recalled Item: Emerge Monorail PTCA Dilatation Catheter. Sterilized using ethylene oxide....

The Issue: Certain dilation and extension catheters are being recalled because these...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2019· Boston Scientific Corporation

Recalled Item: Guidezilla II Guide Extension Catheter Sterilized using ethylene oxide....

The Issue: Certain dilation and extension catheters are being recalled because these...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2019· Applied Medical Resources Corp

Recalled Item: Applied Medical Dual Lumen Graft Cleaning Catheter & 1cc SYRINGE...

The Issue: The firm has received reports of tip separation during usage of the...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 24, 2019· Applied Medical Resources Corp

Recalled Item: Bard Embolectomy Catheter & 1 ml SYRINGE Recalled by Applied Medical...

The Issue: The firm has received reports of tip separation during usage of the...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 24, 2019· Applied Medical Resources Corp

Recalled Item: Python Embolectomy Catheters Recalled by Applied Medical Resources Corp Due...

The Issue: The firm has received reports of tip separation during usage of the...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 23, 2019· Sonendo Inc

Recalled Item: GENTLEWAVE Recalled by Sonendo Inc Due to The console would continue to run...

The Issue: The console would continue to run for extended period when the foot pedal...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 23, 2019· Abbott GmBH & Co. KG

Recalled Item: Alinity c Carbon Dioxide Reagent Kit Recalled by Abbott GmBH & Co. KG Due to...

The Issue: Abbott internal studies have determined that atmospheric Carbon Dioxide...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 22, 2019· Steris Corporation

Recalled Item: Evolution Loading Car and Transfer Carriage- Accessory to the Sterilizer...

The Issue: The locking pin of the front wheel asse mbly of the Evolution Transfer...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 22, 2019· Steris Corporation

Recalled Item: Eagle 3000 Sterilizer Recalled by Steris Corporation Due to Potential for...

The Issue: Potential for the incorrect pressure safety valve being included in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 22, 2019· Edwards Lifesciences, LLC

Recalled Item: EZ Glide Aortic Cannula Recalled by Edwards Lifesciences, LLC Due to Their...

The Issue: Their is a possibility that the cannula may separate from its connector,...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 22, 2019· Encore Medical, LP

Recalled Item: EMPOWR Acetabular System Recalled by Encore Medical, LP Due to The firm...

The Issue: The firm received complaints that the EMPOWR Acetabular Impactor Balls were...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2019· Haemonetics Corporation

Recalled Item: CS5/5+ Fastpacks Recalled by Haemonetics Corporation Due to Potential to...

The Issue: Potential to develop leaks at the inner core of Cell Saver¿ 5/5+ and Cell...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2019· Haemonetics Corporation

Recalled Item: JAPAN CS ELITE FASTPACK Recalled by Haemonetics Corporation Due to Potential...

The Issue: Potential to develop leaks at the inner core of Cell Saver¿ 5/5+ and Cell...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2019· Haemonetics Corporation

Recalled Item: JAPAN BASIC HI SPEED CS5 SET Recalled by Haemonetics Corporation Due to...

The Issue: Potential to develop leaks at the inner core of Cell Saver¿ 5/5+ and Cell...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2019· Haemonetics Corporation

Recalled Item: Cell Saver¿5/5+ Bowl Kit (225 ml) Autotransfusion Device - Product Recalled...

The Issue: Potential to develop leaks at the inner core of Cell Saver¿ 5/5+ and Cell...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2019· Haemonetics Corporation

Recalled Item: CS Elite Fastpack Recalled by Haemonetics Corporation Due to Potential to...

The Issue: Potential to develop leaks at the inner core of Cell Saver¿ 5/5+ and Cell...

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

Class II — Potential Health HazardOngoing