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. 2,869 recalls have been distributed to Pennsylvania in the last 12 months.
Showing 6601–6620 of 55,602 recalls
Recalled Item: RayStation 14.0.0.3338. Radiation Therapy Treatment Planning System....
The Issue: Potential for reported SSD to be too high.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation 9.1.0.933 and 9.2.0.483. Radiation Therapy Treatment Planning...
The Issue: Potential for reported SSD to be too high.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NexGen CR-Flex Femoral Component Recalled by Zimmer, Inc. Due to Out of...
The Issue: Out of specification violation of devices that results in a gap existing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Wegmans brand Frozen Cut Green Beans Recalled by NORTERA FOODS USA Due to...
The Issue: Product may contain foreign object that appears to be of rodent origin.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Aromitalia Malasia Coconut Paste + 35.27 oz milk-based mix Recalled by...
The Issue: Coconut is declared in the ingredient list, but not declared in the contains...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: NEXLIZET (bempedoic acid and ezetimibe) tablets Recalled by Esperion Due to...
The Issue: Failed dissolution specifications: out-of-specification bempedoic acid...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lansoprazole Delayed-Release Capsules USP Recalled by NATCO Pharma Limited...
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Newport s N-LHP-928(j) units if sold as a laser head/power supply set...
The Issue: According to 21 CFR 1040.10(f)(4), each laser system classified as a Class...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Jackson-Pratt 3-Spring Reservoir with Silicone Adapters Recalled by Cardinal...
The Issue: Cardinal Health is issuing a lot number specific voluntary removal of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Jackson-Pratt 3-Spring Reservoir Kit with PVC Round Drain Recalled by...
The Issue: Cardinal Health is issuing a lot number specific voluntary removal of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Jackson-Pratt Universal Connector PVC Tubing Anti Transparent Y Recalled by...
The Issue: Cardinal Health is issuing a lot number specific voluntary removal of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Jackson-Pratt 3-Spring Reservoir Kit with PVC Round Drain Recalled by...
The Issue: Cardinal Health is issuing a lot number specific voluntary removal of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Jackson-Pratt 3-Spring Reservoir Kit with PVC Round Drain Recalled by...
The Issue: Cardinal Health is issuing a lot number specific voluntary removal of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ipratropium Bromide and Albuterol Sulfate Inhalation Solution USP Recalled...
The Issue: Short fill: Complaints received of less fill volume in respule and few drops...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Diltiazem Hydrochloride Extended-Release Capsules Recalled by Glenmark...
The Issue: Failed Dissolution Specifications: Out of Specification (OOS) was reported...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BiPAP V30 Auto Ventilator Recalled by Philips Respironics, Inc. Due to...
The Issue: Potential for devices to experience interruption/loss of therapy during a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BiPAP A40 Ventilators: BiPAP A40 Recalled by Philips Respironics, Inc. Due...
The Issue: Potential for devices to experience interruption/loss of therapy during a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BiPAP A30 Ventilator Recalled by Philips Respironics, Inc. Due to Potential...
The Issue: Potential for devices to experience interruption/loss of therapy during a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stealth S8 Clinical Software Application Recalled by Medtronic Navigation,...
The Issue: Due to a software issue, there is the potential for a missing digit, letter,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: POLYSIN (Polyglycolic Acid) suture Recalled by SURGICAL SPECIALTIES Due to...
The Issue: Complaints have been received with allegations of Incorrect Needle Curvature.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.