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. 2,768 recalls have been distributed to Pennsylvania in the last 12 months.
Showing 17481–17500 of 29,947 recalls
Recalled Item: Truth Renew Plus Recalled by Accord Media, LLC Due to Distribution of...
The Issue: Distribution of medical devices with unapproved green LED light used to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultra Renew Recalled by Accord Media, LLC Due to Distribution of medical...
The Issue: Distribution of medical devices with unapproved green LED light used to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultra Renew Plus Recalled by Accord Media, LLC Due to Distribution of...
The Issue: Distribution of medical devices with unapproved green LED light used to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sundream 12 V tanning bed Recalled by ProSun International, LLC Due to The...
The Issue: The 30 minute maximum tanning time has been reduced to 20 minutes.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Volumat MC Agilia Volumetric Infusion Pump Recalled by Fresenius Vial Sa Due...
The Issue: Fresenius Kabi initiated a mandatory software upgrade of the Volumat MC...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gas Module 3 monitoring spirometer Recalled by Mindray DS USA, Inc. dba...
The Issue: The firm made multiple changes to the product requiring the submission of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rotating IV Pole Rotating IV Pole falls under the category Recalled by...
The Issue: There is the potential for the Rotating IV Pole to fall. A fall could result...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ELEKTA Digital Accelerator under the following brand names: Elekta Synergy...
The Issue: There is a potential for an uncontrolled extension of iViewGT / XVI detector...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RESTORIS MCK TIBIAL BASEPLATE-RM/LL used in unicompartmental knee...
The Issue: Incorrect product and/or label. Sizing is labeled incorrectly.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VERSYS 7.5 IN BEADED FC +10 CALCAR 13.5X180MM STR +10 Recalled by Zimmer...
The Issue: The LDPE bag packaging for various highly polished hip and knee implants may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BCI Advisor Vital Signs Monitor Recalled by Smiths Medical ASD Inc. Due to...
The Issue: Some printing modes on the devices may not function properly (tabular data...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Persona Partial Knee spacer block instruments Recalled by Zimmer Biomet,...
The Issue: Certain partial knee implant spacer blocks do not fit in the alignment tower...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tapered Screw-Vent MTX Recalled by Zimmer Dental Inc Due to Mislabeling
The Issue: Two lots of the Tapered Screw-Vent Implants, with different outer thread...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tapered Screw-Vent MTX Recalled by Zimmer Dental Inc Due to Mislabeling
The Issue: Two lots of the Tapered Screw-Vent Implants, with different outer thread...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CPT 12/14 COCR SIZE 0 STD prosthesis Recalled by Zimmer Biomet, Inc. Due to...
The Issue: The LDPE bag packaging for various highly polished hip and knee implants may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VERSYS 6 INCH BEADED FC 13X160MM LM BODY EXT NECK & STD NECK Prosthesis...
The Issue: The LDPE bag packaging for various highly polished hip and knee implants may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LPS PRECOAT FEM SIZE D-RT LPS PRECOAT FEM SIZE E-RT Recalled by Zimmer...
The Issue: The LDPE bag packaging for various highly polished hip and knee implants may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CR OPTION FEM COMP SIZE C/L CR OPTION FEM COMP Recalled by Zimmer Biomet,...
The Issue: The LDPE bag packaging for various highly polished hip and knee implants may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LPS-FLEX OPTION FEMORAL C-L LPS-FLEX OPTION FEMORAL C-L LPS-FLEX OPTION...
The Issue: The LDPE bag packaging for various highly polished hip and knee implants may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CR-FLEX POR HATCP FEM C-L CR-FLEX POR HATCP FEM C-R Recalled by Zimmer...
The Issue: The LDPE bag packaging for various highly polished hip and knee implants may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.