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. 1,017 recalls have been distributed to Pennsylvania in the last 12 months.
Showing 36661–36680 of 55,602 recalls
Recalled Item: Light Adaptor for Small Battery Drive and Small Battery Drive II. Recalled...
The Issue: There was a potential for the Adaptor and Light Adaptor for Small Battery...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Roadrunner Uniglide Hydrophilic Wire Guide Recalled by Cook Inc. Due to...
The Issue: Potential coating contamination with glass particles.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Adaptor for Small Battery Drive and Small Battery Drive II. Recalled by The...
The Issue: There was a potential for the Adaptor and Light Adaptor for Small Battery...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Amoxicillin for Oral Suspension USP Recalled by Teva North America Due to...
The Issue: Superpotent drug: Out of specification test result for assay during...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Figi's Gifts in Good Taste Recalled by Figi's, Inc Due to Potential Listeria...
The Issue: Figi's Companies, Inc is recalling 2 products that are related to the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Snack Shoppe Recalled by Figi's, Inc Due to Potential Listeria Contamination
The Issue: Figi's Companies, Inc is recalling 2 products that are related to the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: 2.3MM Tapered Router Recalled by Stryker Instruments Div. of Stryker...
The Issue: A variation in flute depth on the routers was observed. The variation in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Trucount Tubes: Catalog number: 340334 Hematology: BD Trucount tubes...
The Issue: One lot of BD Trucount Absolute Counting Tubes (IVD) may not be sealed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optical Surface Monitoring System{OSMS Recalled by Varian Medical Systems,...
The Issue: Varian Medical Systems has received reports that unintended changes were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Syngo.via Recalled by Siemens Medical Solutions USA, Inc Due to Incorrect...
The Issue: Incorrect values for the volume calculation. Software update VB30B via...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optical Surface Monitoring System{Align RT Plus} This is used on Recalled by...
The Issue: Varian Medical Systems has received reports that unintended changes were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diazepam Injection USP 10mg/2mL (5 mg/mL Recalled by Hospira Inc. Due to...
The Issue: Crystallization: Product contains particulate identified to be crystallized...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: AUTOCOMP6 XPS High Speed Compounder Recalled by The Metrix Company Due to An...
The Issue: An issue was identified after a redesign of the auto compounding device. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mindray DS USA Inc. Recalled by Mindray DS USA, Inc. dba Mindray North...
The Issue: Mindray has identified a potential leakage issue with the CO2 Module's...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dual Chamber Container fill with gravity/attached transfer sets Recalled by...
The Issue: An issue was identified after a redesign of the auto compounding device. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AUTOCOMP6 High Speed Compounder Recalled by The Metrix Company Due to An...
The Issue: An issue was identified after a redesign of the auto compounding device. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Container fill and transfer sets Recalled by The Metrix Company Due to An...
The Issue: An issue was identified after a redesign of the auto compounding device. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EtCO2 Module -Part Number: 02.01.210699 Monitors: iM80 Recalled by Edan...
The Issue: Incorrect CO2 readings with some patient monitors.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dual Chamber Container fill and transfer sets Recalled by The Metrix Company...
The Issue: An issue was identified after a redesign of the auto compounding device. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Container fill and transfer sets Recalled by The Metrix Company Due to An...
The Issue: An issue was identified after a redesign of the auto compounding device. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.