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. 2,696 recalls have been distributed to Pennsylvania in the last 12 months.
Showing 22161–22180 of 29,947 recalls
Recalled Item: GE Healthcare Recalled by GE Medical Systems, LLC Due to The Drive Gas Check...
The Issue: The Drive Gas Check Valve of certain Anesthesia products could become stuck...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Medical Systems, LLC Due to The Drive Gas Check...
The Issue: The Drive Gas Check Valve of certain Anesthesia products could become stuck...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: D-10 Rack Loader Recalled by Bio-Rad Laboratories, Inc. Due to On a rare...
The Issue: On a rare occasion, there is a potential to assign a patient result to an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Medical Systems, LLC Due to The Drive Gas Check...
The Issue: The Drive Gas Check Valve of certain Anesthesia products could become stuck...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Medical Systems, LLC Due to The Drive Gas Check...
The Issue: The Drive Gas Check Valve of certain Anesthesia products could become stuck...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Panorama Patient Monitoring Network. Software Kit 0020-00-0205-19A Recalled...
The Issue: An issue with the Panorama Central Station may cause the system to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FMC7 FITC Recalled by Becton, Dickinson and Company, BD Biosciences Due to...
The Issue: Becton, Dickinson and Company (BD) has determined that the FMC7 FITC (ASR)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CDI¿ H/S Cuvette The intended use for the CDI¿ H Recalled by Terumo...
The Issue: Terumo Cardiovascular Systems (Terumo CVS) has received complaints of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ascom Mobile Monitoring Gateway (versions 4.1.1 and 4.2.0) and Ascom...
The Issue: Due to a malfunction of software, the secondary module will not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flow-i Anesthesia System Product Usage: The indication for the Flow-i...
The Issue: Electrical issues in the control, monitoring or panel sub-systems, caused by...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IBA Dosimetry GmbH Lift Table Type 4320 Recalled by Iba Dosimetry Gmbh Due...
The Issue: When the electric lift table is connected to the mains power, in a very rare...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Periarticular Locking Plate System 3.5mm Locking Screw 58 mm Length...
The Issue: Product on the package label did not match what was inside the package. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MOSAIQ Oncology Information System MOSAIQ is an oncology information system...
The Issue: Incorrect drug dosage due to "Age Limit" and patient weight data item issue.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Perkin Elmer WIZARD2 10-detector Recalled by Perkinelmer Due to The content...
The Issue: The content of the second #023 barcode ID label in the Barcode ID Label...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Perkin Elmer WIZARD2 5-detector Recalled by Perkinelmer Due to The content...
The Issue: The content of the second #023 barcode ID label in the Barcode ID Label...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Perkin Elmer WIZARD2 10-detector Recalled by Perkinelmer Due to The content...
The Issue: The content of the second #023 barcode ID label in the Barcode ID Label...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Perkin Elmer WIZARD2 1-detector Recalled by Perkinelmer Due to The content...
The Issue: The content of the second #023 barcode ID label in the Barcode ID Label...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Perkin Elmer WIZARD2 1-detector Recalled by Perkinelmer Due to The content...
The Issue: The content of the second #023 barcode ID label in the Barcode ID Label...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AltiVate Reverse Humeral Broach Recalled by Encore Medical, Lp Due to The...
The Issue: The trial shell mating feature on the broach is undersized.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Perkin Elmer WIZARD2 2-detector Recalled by Perkinelmer Due to The content...
The Issue: The content of the second #023 barcode ID label in the Barcode ID Label...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.