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 28921–28940 of 29,947 recalls
Recalled Item: IDS-iSYS Ostase¿ BAP (Bone Alkaline Phosphatase) Recalled by...
The Issue: It has been noted by staff at IDS Inc. that stock of the affected products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IDS-iSYS N-Mid¿ Osteocalcin Recalled by Immunodiagnostics Systems Ltd Due to...
The Issue: It has been noted by staff at IDS Inc. that stock of the affected products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IDS-iSYS Ostase¿ BAP (Bone Alkaline Phosphatase) Control Set Recalled by...
The Issue: It has been noted by staff at IDS Inc. that stock of the affected products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IDS-iSYS Intact PINP Recalled by Immunodiagnostics Systems Ltd Due to It has...
The Issue: It has been noted by staff at IDS Inc. that stock of the affected products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QKC1692E The QKC1692E Quick Connect device connects endoscopes to the...
The Issue: STERIS has been actively seeking devices for quick connect revalidation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IDS-iSYS N-Mid¿ Osteocalcin Recalled by Immunodiagnostics Systems Ltd Due to...
The Issue: It has been noted by staff at IDS Inc. that stock of the affected products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Capsule Neuron Docking Station Recalled by Capsule Tech Inc. Due to Capsule...
The Issue: Capsule Neuron Docking Station may experience a lost connection, resulting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MyRay RXDC dental unit x-ray unit Recalled by CEFLA DENTAL GROUP Due to The...
The Issue: The RX DC dental x-ray unit was found to be noncompliant with 21CFR 1010,2,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra HRAIM Head Ring Assembly with Intubation Mounts The CRW Recalled by...
The Issue: T-handle screw is used on a complementary product to the CRW, the Integra...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Omnilife Science Apex Knee System Modular Tibia Augment Recalled by Omni...
The Issue: The Apex Knee System Modular Tibia Augment may breach the inner and outer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Omnilife Science Apex Knee System Modular Tibia Augment Recalled by Omni...
The Issue: The Apex Knee System Modular Tibia Augment may breach the inner and outer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra CRW Precision Arc (CRWPRECISE) Recalled by Integra LifeSciences...
The Issue: T-handle screw is used on a complementary product to the CRW, the Integra...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biliary Catheters (Models A47XX and CB0XXXXX): Model Numbers & Description:...
The Issue: Applied Medical is recalling specific lot numbers of its Vascular Catheters...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista(R) Systems Vista(R) Theophylline THEO Flex(R) Regent...
The Issue: Firm has received complaints from customers of "Abnormal Reaction" errors...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Embolectomy Catheters (Models A44XX Recalled by Applied Medical Resources...
The Issue: Applied Medical is recalling specific lot numbers of its Vascular Catheters...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker MANTIS TORQUE WRENCH Manufactured by: Stryker pine Recalled by...
The Issue: Multiple complaints have reported the hex tip of the torque wrench...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Omnilife Science Apex Knee System Modular Tibia Augment Recalled by Omni...
The Issue: The Apex Knee System Modular Tibia Augment may breach the inner and outer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SPECIALTY AUDIBLE TORQUE WRENCH Recalled by Stryker Spine Due to Multiple...
The Issue: Multiple complaints have reported the hex tip of the torque wrench...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Omnilife Science Apex Knee System Modular Tibia Augment Recalled by Omni...
The Issue: The Apex Knee System Modular Tibia Augment may breach the inner and outer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AmeriWater MRO Dialysis RO+ System Recalled by AmeriWater Inc Due to The...
The Issue: The firm was notified that a malfunction of the device was caused by an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.