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. 2,679 recalls have been distributed to Pennsylvania in the last 12 months.
Showing 26781–26800 of 29,947 recalls
Recalled Item: Dual Luer Lock Cap The device is intended for use Recalled by Baxter...
The Issue: The firm is recalling lots 10043 and 10044 due to loose particulate matter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ready to Use Thymo-Cide Recalled by Wexford Labs Inc Due to Expired active...
The Issue: Expired active ingredient was used in the manufacture of the product.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith Medical Recalled by Smiths Medical ASD, Inc. Due to Smiths Medical is...
The Issue: Smiths Medical is conducting a voluntary recall of PORT-A-CATH¿ and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hospira RECEPTAL LINERS: 1L(1000mL) Recalled by Hospira Inc. Due to Hospira...
The Issue: Hospira has become aware of customers using the incorrect size Receptal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hospira RECEPTAL CANISTERS: 1L(1000mL) Recalled by Hospira Inc. Due to...
The Issue: Hospira has become aware of customers using the incorrect size Receptal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: *** 1) Product labeled in part: List No. 14220-28 Recalled by Hospira Inc....
The Issue: Intravenous fluid may leak at the CLAVE secondary port of Hospira PlumSet IV...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: *** 1) Product labeled in part: 19683-28 Recalled by Hospira Inc. Due to...
The Issue: Intravenous fluid may leak at the CLAVE secondary port of Hospira PlumSet IV...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: *** 1) Product labeled in part: 14951-48 Recalled by Hospira Inc. Due to...
The Issue: Intravenous fluid may leak at the CLAVE secondary port of Hospira PlumSet IV...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: *** 1) Product labeled in part: List No. 14212-28 Recalled by Hospira Inc....
The Issue: Intravenous fluid may leak at the CLAVE secondary port of Hospira PlumSet IV...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: *** 1) Product labeled in part: 19734-28 Recalled by Hospira Inc. Due to...
The Issue: Intravenous fluid may leak at the CLAVE secondary port of Hospira PlumSet IV...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ISE Recalled by Beckman Coulter Inc. Due to The recall was initiated because...
The Issue: The recall was initiated because Beckman Coulter has confirmed that some AU...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BBL (tm) MGIT (tm) Mycobacteria Growth Indicator Tube Recalled by Becton...
The Issue: An in-vitro diagnostic reagent may be labeled with an incorrect barcode,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ISE Recalled by Beckman Coulter Inc. Due to The recall was initiated because...
The Issue: The recall was initiated because Beckman Coulter has confirmed that some AU...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Small Bone Innovations (SBi) rHead Radial Stem Recalled by Small Bone...
The Issue: The recall was initiated due to an increased risk of implants breaching the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: chromID Salmonella Agar Recalled by bioMerieux, Inc. Due to Potential...
The Issue: Complaints for Salmonella strains growing on this medium producing an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Selenia Full Field Digital Mammography System with software versions 5.0.x...
The Issue: Software: When the Selenia upon meeting the hard drive threshold of 4,000...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DROP-ARM CONVALESCENT RECLINER 5271/5281 with One-touch release for...
The Issue: A supplier manufacturing assembly defect with the right hand recline...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CONVALESCENT RECLINER 5251/5261 Recalled by Winco Mfg., LLC Due to A...
The Issue: A supplier manufacturing assembly defect with the right hand recline...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PREMIER CARE RECLINER 5570 with Urethane armrests Recalled by Winco Mfg.,...
The Issue: A supplier manufacturing assembly defect with the right hand recline...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: XL CONVALESCENT RECLINER 5291/529S with Padded armrests with guard Recalled...
The Issue: A supplier manufacturing assembly defect with the right hand recline...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.