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. 991 recalls have been distributed to Pennsylvania in the last 12 months.
Showing 41061–41080 of 55,602 recalls
Recalled Item: Synthes Trauma Ex-Fix System (Small Recalled by Synthes (USA) Products LLC...
The Issue: Labeling changes were made related to MR conditions that align with standard...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NovaPlus Trach Care* Closed Suction System for Adults Recalled by Halyard...
The Issue: The thumb valve of some KIMVENT Closed Suction Systems remained partially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KimVent* Closed Suction System for Adults Recalled by Halyard Health, Inc...
The Issue: The thumb valve of some KIMVENT Closed Suction Systems remained partially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KimVent* Closed Suction System for Adults Recalled by Halyard Health, Inc...
The Issue: The thumb valve of some KIMVENT Closed Suction Systems remained partially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KimVent* Turbo-Cleaning Closed Suction System for Adults Recalled by Halyard...
The Issue: The thumb valve of some KIMVENT Closed Suction Systems remained partially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KimVent* Closed Suction System for Adults Recalled by Halyard Health, Inc...
The Issue: The thumb valve of some KIMVENT Closed Suction Systems remained partially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KimVent* Closed Suction System for Adults Recalled by Halyard Health, Inc...
The Issue: The thumb valve of some KIMVENT Closed Suction Systems remained partially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KimVent* Closed Suction System for Adults Recalled by Halyard Health, Inc...
The Issue: The thumb valve of some KIMVENT Closed Suction Systems remained partially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lisinopril Tablets Recalled by Vintage Pharmaceuticals LLC dba Qualitest...
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lisinopril Tablets USP Recalled by Wockhardt Usa Inc. Due to CGMP...
The Issue: CGMP Deviations: An FDA inspection identified inadequate investigations of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lisinopril Tablets USP Recalled by Wockhardt Usa Inc. Due to CGMP...
The Issue: CGMP Deviations: An FDA inspection identified inadequate investigations of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Software version 4.44A utilized on the BD MAX System Recalled by BD LIFE...
The Issue: The BD MAX System software version 4.44A contains a software anomaly that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TopCare LORATIDINE ORALLY DISINTEGRATING TABLETS Recalled by Ohm...
The Issue: Superpotent Drug: Out Of Specification (OOS) result for Assay.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Hydralazine Hydrochloride Injection Recalled by Fresenius Kabi USA, LLC Due...
The Issue: Incorrect Expiration Date: The "11/06" expiration date printed on the tray...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Leader Loratadine Orally Disintegrating Tablets Recalled by Ohm...
The Issue: Superpotent Drug: Out Of Specification (OOS) result for Assay.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sunmark loratadine Orally Disintegrating Tablets Recalled by Ohm...
The Issue: Superpotent Drug: Out Of Specification (OOS) result for Assay.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Safeway Care Loratadine Orally Disintegrating Tablets Recalled by Ohm...
The Issue: Superpotent Drug: Out Of Specification (OOS) result for Assay.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Health Mart Pharmacy loratadine orally disintegrating tablets Recalled by...
The Issue: Superpotent Drug: Out Of Specification (OOS) result for Assay.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ohm Loratadine Orally Disintegrating Tablets Recalled by Ohm Laboratories,...
The Issue: Superpotent Drug: Out Of Specification (OOS) result for Assay.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Discount Drug Mart Food Fair Recalled by Ohm Laboratories, Inc. Due to...
The Issue: Superpotent Drug: Out Of Specification (OOS) result for Assay.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.