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. 1,810 recalls have been distributed to Pennsylvania in the last 12 months.

55,602 total recalls
1,810 in last 12 months

Showing 5536155380 of 55,602 recalls

Medical DeviceApril 1, 2011· Zimmer, Inc.

Recalled Item: 12/14 Neck Taper 00789504001 VerSys Femoral Head Provisional 40mm -3.5...

The Issue: Complaints have been received reporting sub-optimal fit between provisional...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2011· Zimmer, Inc.

Recalled Item: 00780304001 MIS 12/14 Slotted Femoral Head Provisional -3.5X36 00780304002...

The Issue: Complaints have been received reporting sub-optimal fit between provisional...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2011· Zimmer, Inc.

Recalled Item: 00789502801 VerSys Femoral Head Provisional 28mm -3.5 00789502802 VerSys...

The Issue: Complaints have been received reporting sub-optimal fit between provisional...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2011· Zimmer, Inc.

Recalled Item: 00780302601 MIS 12/14 Slotted Femoral Head Provisional -3.5X26 00780302602...

The Issue: Complaints have been received reporting sub-optimal fit between provisional...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2011· Zimmer, Inc.

Recalled Item: 12/14 Neck Taper 00789503201 VerSys Femoral Head Provisional 32mm -3.5...

The Issue: Complaints have been received reporting sub-optimal fit between provisional...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2011· Zimmer, Inc.

Recalled Item: 00789503601 VerSys Femoral Head Provisional 36mm -3.5 00789503602 VerSys...

The Issue: Complaints have been received reporting sub-optimal fit between provisional...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2011· GE Healthcare, LLC

Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to When performing a...

The Issue: When performing a secondary capture generated from GSI Viewer, the header...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2011· Clinical Diagnostic Solutions

Recalled Item: Boule Con-Diff Hematology Control For in vitro diagnostic use as Recalled by...

The Issue: Clinical Diagnostic Solutions, Inc. in Plantation, FL recalled Boule Con...

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

Class III — Low RiskOngoing
Medical DeviceMarch 24, 2011· Clinical Diagnostic Solutions

Recalled Item: Boule Con-Diff Hematology Control For in vitro diagnostic use as Recalled by...

The Issue: Clinical Diagnostic Solutions, Inc. in Plantation, FL recalled Boule Con...

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

Class III — Low RiskOngoing
Medical DeviceMarch 24, 2011· Clinical Diagnostic Solutions

Recalled Item: Boule Con-Diff Hematology Control For in vitro diagnostic use as Recalled by...

The Issue: Clinical Diagnostic Solutions, Inc. in Plantation, FL recalled Boule Con...

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

Class III — Low RiskOngoing
Medical DeviceMarch 21, 2011· Stryker Spine

Recalled Item: Stryker Reliance AL Implant Blocker (Various sizes) The SLIDE Implant...

The Issue: Stryker Spine has received six reports regarding the breakage of one or more...

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

Class II — Potential Health HazardOngoing
DrugMarch 18, 2011· Physicians Total Care, Inc.

Recalled Item: Methylprednisolone Tablets Recalled by Physicians Total Care, Inc. Due to...

The Issue: Impurities/Degradation Products; Product is being recalled due to the...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 16, 2011· Hospira Inc.

Recalled Item: Symbiq Two Channel Infuser Recalled by Hospira Inc. Due to May go to a white...

The Issue: May go to a white screen due to a problem with the SOM2 module. A white...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2011· Hospira Inc.

Recalled Item: Symbiq One Channel Infuser Recalled by Hospira Inc. Due to May go to a white...

The Issue: May go to a white screen due to a problem with the SOM2 module. A white...

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

Class II — Potential Health HazardOngoing
DrugMarch 15, 2011· Luitpold Pharmaceuticals, Inc.

Recalled Item: CONCENTRATED SODIUM CHLORIDE INJECTION Recalled by Luitpold Pharmaceuticals,...

The Issue: Presence of Particulate Matter: In the course of inspecting retention...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 9, 2011· Biomet Spine LLC.

Recalled Item: LANX Recalled by Biomet Spine LLC. Due to Biomet Spine, LLC. announces...

The Issue: Biomet Spine, LLC. announces voluntary recall of Durango Anchored ALIF Plate...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2011· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance iCT Recalled by Philips Medical Systems (Cleveland) Inc Due to...

The Issue: The DoseRight feature suggest a mAs based on the measured patient size, a...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2011· Ge Healthcare It

Recalled Item: Imagecast PACS is an image management system intended to be Recalled by Ge...

The Issue: In Imagecast PACS versions prior to 3.6.51.01, the estimated magnification...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2011· The Anspach Effort, Inc.

Recalled Item: ****** 3mm Diamond Ball. Used for cutting and shaping bone. Recalled by The...

The Issue: Due to three batches of product may have diamond grit size larger than...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2011· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance 64 Computed Tomography X-Ray System Recalled by Philips Medical...

The Issue: Multiple software defects which could impact the performance or reliability...

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

Class II — Potential Health HazardOngoing