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 2464124660 of 29,947 recalls

Medical DeviceOctober 17, 2014· Biomet Microfixation, LLC

Recalled Item: Total Temporomandibular Joint Replacement System- 45mm Lft Standard 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· Biomet Microfixation, LLC

Recalled Item: Total Temporomandibular Joint Replacement System- 50mm Rt Standard 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· Biomet Microfixation, LLC

Recalled Item: Total Temporomandibular Joint Replacement System- 50mm Rt 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· Maquet Cardiovascular Us Sales, Llc

Recalled Item: Cardiohelp-I System Product Usage: A blood oxygenation and carbon dioxide...

The Issue: Cardiohelp- i System may have a software issue that can potentially result...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2014· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Rapid Neg BP Combo Panel Type 3 Recalled by Siemens Healthcare Diagnostics,...

The Issue: An increase in false positive susceptible results on Rapid Neg BP Combo...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 17, 2014· Biomet Microfixation, LLC

Recalled Item: Total Temporomandibular Joint Replacement System- 55mm Rt Standard 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· Biomet Microfixation, LLC

Recalled Item: Total Temporomandibular Joint Replacement System- 45mm Rt Stand Off TI...

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· Biomet Microfixation, LLC

Recalled Item: Total Temporomandibular Joint Replacement System- 45mm Rt 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
Medical DeviceOctober 17, 2014· Ethicon, Inc.

Recalled Item: Ethicon PERMA-HAND Silk siliconized black braided 10 strands per packet...

The Issue: Ethicon is unable to ensure that PERMA-HAND silk suture (siliconized black...

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- 45mm Rt Standard 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 16, 2014· Materialise USA LLC

Recalled Item: Zimmer Patient Specific Instrument PERSONA CR Pin Guides (Femur and Recalled...

The Issue: The box of guides for a specific case arrived intact but contained two (2)...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2014· Skeletal Dynamics

Recalled Item: Align Radial Stems Recalled by Skeletal Dynamics Due to Report received...

The Issue: Report received where the Align Radial Stem fractured.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2014· Diagnostic Hybrids Inc

Recalled Item: MicroVue Bb Plus EIA is packaged as a kit which Recalled by Diagnostic...

The Issue: Samples are quantitating incorrectly, with approximately 50% higher...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2014· Biomerieux

Recalled Item: Etest¿ Ceftaroline (CPT32) US B30. Etest¿ (Antimicrobial Susceptibility...

The Issue: The products have a wrong expiration date on their labeling, 5 years instead...

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

Class III — Low RiskOngoing
Medical DeviceOctober 16, 2014· Biomerieux

Recalled Item: Etest¿ Ceftaroline (CPT32) US B100. Etest¿ (Antimicrobial Susceptibility...

The Issue: The products have a wrong expiration date on their labeling, 5 years instead...

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

Class III — Low RiskOngoing
Medical DeviceOctober 16, 2014· Biomerieux

Recalled Item: Etest¿ Ceftaroline (CPT32) WW B30. Etest¿ (Antimicrobial Susceptibility...

The Issue: The products have a wrong expiration date on their labeling, 5 years instead...

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

Class III — Low RiskOngoing
Medical DeviceOctober 16, 2014· Biomerieux

Recalled Item: Etest¿ Ceftaroline (CPT32) US B30. Etest¿ (Antimicrobial Susceptibility...

The Issue: The products have a wrong expiration date on their labeling, 5 years instead...

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

Class III — Low RiskOngoing
Medical DeviceOctober 16, 2014· Biomerieux

Recalled Item: Etest¿ Ceftaroline (CPT32) WWB100. Etest¿ (Antimicrobial Susceptibility...

The Issue: The products have a wrong expiration date on their labeling, 5 years instead...

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

Class III — Low RiskOngoing
Medical DeviceOctober 15, 2014· American Medical Systems, Inc.

Recalled Item: AMS Monarc + Subfascial Hammock with Tensioning Suture Recalled by American...

The Issue: During routine periodic packaging testing, AMS identified that in simulated...

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

Class II — Potential Health HazardOngoing