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. 968 recalls have been distributed to Pennsylvania in the last 12 months.

55,602 total recalls
968 in last 12 months

Showing 45321–45340 of 55,602 recalls

Medical DeviceOctober 21, 2014· Gyrus Acmi, Incorporated

Recalled Item: Gyrus ACMI Disposable Falope-Ring Band Applicator Kits. and Recalled by...

The Issue: All packages of Falope Ring Band Applicator kits are being recalled due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2014· Diamedix Corporation

Recalled Item: Diamedix Is-EBV-EA-D IgG Test Kit Diamedix Is-Mumps IgG Test Kit Recalled by...

The Issue: A gel-like substance was found in kit component, sample diluent , that could...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2014· Pfm Medical Inc

Recalled Item: Thoracentesis & Paracentesis Procedure Tray Recalled by Pfm Medical Inc Due...

The Issue: PFM Medical is recalling catheters and other medical devices because they...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2014· Pfm Medical Inc

Recalled Item: ASEPT 2000 ml Drainage Bag Recalled by Pfm Medical Inc Due to PFM Medical is...

The Issue: PFM Medical is recalling catheters and other medical devices because they...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2014· Microgenics Corporation

Recalled Item: MAS CardioImmune XL Cardiac Marker Control Recalled by Microgenics...

The Issue: MAS CardioImmune XL, level 1 (lot CXL16011), is showing vial-to-vial...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2014· Pfm Medical Inc

Recalled Item: ASEPT 600 ml Drainage Kit Recalled by Pfm Medical Inc Due to PFM Medical is...

The Issue: PFM Medical is recalling catheters and other medical devices because they...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2014· Pfm Medical Inc

Recalled Item: Micro Introducer Kit Recalled by Pfm Medical Inc Due to PFM Medical is...

The Issue: PFM Medical is recalling catheters and other medical devices because they...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2014· Pfm Medical Inc

Recalled Item: 6F x 60 cm Dual Lumen CT PICC Recalled by Pfm Medical Inc Due to PFM Medical...

The Issue: PFM Medical is recalling catheters and other medical devices because they...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2014· Pfm Medical Inc

Recalled Item: Rapid Centesis Catheter Recalled by Pfm Medical Inc Due to PFM Medical is...

The Issue: PFM Medical is recalling catheters and other medical devices because they...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2014· Pfm Medical Inc

Recalled Item: ASEPT Peritoneal Drainage System Recalled by Pfm Medical Inc Due to PFM...

The Issue: PFM Medical is recalling catheters and other medical devices because they...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2014· Pfm Medical Inc

Recalled Item: Veta Peritoneal Catheter Kit Recalled by Pfm Medical Inc Due to PFM Medical...

The Issue: PFM Medical is recalling catheters and other medical devices because they...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2014· Diamedix Corporation

Recalled Item: Diamedix Is-EBV-VCA IgG Test Kit Diamedix Is-Mumps IgG Test Kit Recalled by...

The Issue: A gel-like substance was found in kit component, sample diluent , that could...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2014· Radiometer America Inc

Recalled Item: HemoCue¿ Glucose 201 Microcuvettes Recalled by Radiometer America Inc Due to...

The Issue: Batches of HemoCue Glucose 201 Microcuvettes show discoloration and provide...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2014· Diamedix Corporation

Recalled Item: Diamedix Is-Mumps IgG Test Kit Diamedix Is-Mumps IgG Test Kit Recalled by...

The Issue: A gel-like substance was found in kit component, sample diluent , that could...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2014· Pfm Medical Inc

Recalled Item: ASEPT Pleural Drainage System Recalled by Pfm Medical Inc Due to PFM Medical...

The Issue: PFM Medical is recalling catheters and other medical devices because they...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2014· Siemens Healthcare Diagnostics, Inc.

Recalled Item: IMMULITE Calcitonin Control Module (IMMULITE Recalled by Siemens Healthcare...

The Issue: A typographical error regarding the expiration date was identified in the...

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

Class III — Low RiskOngoing
FoodOctober 20, 2014· Bailey Farms, Inc.

Recalled Item: Bailey Farms Recalled by Bailey Farms, Inc. Due to Potential Salmonella...

The Issue: Product was found to be contaminated with Salmonella

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
Medical DeviceOctober 19, 2014· Biosense Webster, Inc.

Recalled Item: ThermoCool SmartTouch Navigation Catheters Recalled by Biosense Webster,...

The Issue: The recall was initiated because Biosense Webster is providing additional...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2014· Biomet Microfixation, LLC

Recalled Item: Total Temporomandibular Joint Replacement System- 50mm Lft Narrow Ti Mand...

The Issue: Laser etching on the parts is wider and deeper than the conditions...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2014· INO Therapeutics (dba Ikaria)

Recalled Item: INOMAX DSIR Nitric Oxide delivery system Recalled by INO Therapeutics (dba...

The Issue: An issue has been identified in the INOmax DSIR system that could result in...

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

Class II — Potential Health HazardOngoing