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. 1,107 recalls have been distributed to Pennsylvania in the last 12 months.
Showing 14681–14700 of 55,602 recalls
Recalled Item: HCG 6 Recalled by Revive Rx LLC dba Revive Rx Pharmacy Due to Non-sterility;...
The Issue: Non-sterility; bacterial contamination identified as Paenibacillus lautus.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CombiDiagnost R90 1.0 (709030) Recalled by PHILIPS MEDICAL SYSTEMS Due to...
The Issue: While performing a fluoroscopy examination, there is a potential that the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CombiDiagnost R90 1.1 (709031) Recalled by PHILIPS MEDICAL SYSTEMS Due to...
The Issue: While performing a fluoroscopy examination, there is a potential that the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nextra Hammertoe Correction System 4.5 Middle and 3.2 Proximal Saw Recalled...
The Issue: Proximal end of the driver is oversized in varying degrees, making it...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nextra Hammertoe Correction System 4.5 Middle 3.2 Proximal Kit SKU: Recalled...
The Issue: Proximal end of the driver is oversized in varying degrees, making it...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nextra Hammertoe Correction System 3.5 Middle 3.2 Proximal Kit SKU: Recalled...
The Issue: Proximal end of the driver is oversized in varying degrees, making it...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nextra Hammertoe Correction System 3.5 Middle and 3.2 Proximal Saw Recalled...
The Issue: Proximal end of the driver is oversized in varying degrees, making it...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nextra Hammertoe Correction System Driver SKU: NX-DR Orthopedic surgical...
The Issue: Proximal end of the driver is oversized in varying degrees, making it...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Favorite Day Carrot cake soft bake cookies Net Wt 8 Recalled by J & M Foods,...
The Issue: Pecans although listed in the Ingredient Statement, was omitted from the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: RISE UP RED EDITION Capsules Recalled by Positive Health Due to Undeclared...
The Issue: Marketed Without An Approved NDA/ANDA: Product was found to contain...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Avaphinal Maximum Male Enhancement Sexual Pills Recalled by Walmart Stores...
The Issue: Marketed Without An Approved NDA/ANDA: Product was found to contain...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Diazepam Oral Solution (Concentrate) Recalled by Lannett Company, Inc. Due...
The Issue: Failed Impurities/Degradation Specifications: Out of specification results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Atellica CH Fructosamine (Fruc) Recalled by Siemens Healthcare Diagnostics,...
The Issue: Siemens Healthcare Diagnostics Inc. has confirmed the potential for reagent...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica CH Enzymatic Hemoglobin A1c (A1c_E/A1c_H) Recalled by Siemens...
The Issue: Siemens Healthcare Diagnostics Inc. has confirmed the potential for reagent...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VIDAS CMV IgM Recalled by bioMerieux, Inc. Due to Invalid calibrations (out...
The Issue: Invalid calibrations (out of range high) while using the product.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica CH Calcium_2 (CA_2) Recalled by Siemens Healthcare Diagnostics,...
The Issue: Siemens Healthcare Diagnostics Inc. has confirmed the potential for reagent...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultima Activator II Reusable Drive Mechanism Recalled by Maquet...
The Issue: Potential for corrosion on the pins of the Ultima Activator II Reusable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica CH Lithium_2 (LITH_2) Recalled by Siemens Healthcare Diagnostics,...
The Issue: Siemens Healthcare Diagnostics Inc. has confirmed the potential for reagent...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BioPlex 2200 Syphilis Total & RPR Calibrator Set CAL Recalled by Bio-Rad...
The Issue: Due to current concerns related to COVID-19 vaccine interference with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BioPlex 2200 SYPH T PACK Syphilis Total & RPR Reagent Pack Recalled by...
The Issue: Due to current concerns related to COVID-19 vaccine interference with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.