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. 2,165 recalls have been distributed to Pennsylvania in the last 12 months.
Showing 7241–7260 of 29,947 recalls
Recalled Item: Surgical convenience kits labeled as: CENTURION MEDICAL PRODUCTS L & D TRAY...
The Issue: The recall is due to the perforated bag not allowing for outside of the kit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NexGen Option Stemmed Tibial Component Size 6 Recalled by Zimmer, Inc. Due...
The Issue: Zimmer Biomet is conducting a voluntary medical device recall related to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NexGen Option Stemmed Tibial Component Size 8 Recalled by Zimmer, Inc. Due...
The Issue: Zimmer Biomet is conducting a voluntary medical device recall related to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NexGen Option Stemmed Tibial Component Size 5 Recalled by Zimmer, Inc. Due...
The Issue: Zimmer Biomet is conducting a voluntary medical device recall related to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Future Diagnostics STAT-IntraOperative-Intact-PTH (STAT-IO-I-PTH)...
The Issue: Due to an issue of high coefficient of variability (CV) problem caused by...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NexGen Option Stemmed Tibial Component Size 4 Recalled by Zimmer, Inc. Due...
The Issue: Zimmer Biomet is conducting a voluntary medical device recall related to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NexGen Option Stemmed Tibial Component Size 7 Recalled by Zimmer, Inc. Due...
The Issue: Zimmer Biomet is conducting a voluntary medical device recall related to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NexGen Option Stemmed Tibial Component Size 3 Recalled by Zimmer, Inc. Due...
The Issue: Zimmer Biomet is conducting a voluntary medical device recall related to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Denticator PICK-A-DENT Recalled by Young Dental Manufacturing I, LLC Due to...
The Issue: mislabeled product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Turbett Surgical Container Recalled by Turbett Surgical, Inc. Due to Pod may...
The Issue: Pod may have weld failures breaching the sterile barrier and result in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SHIP KIT Recalled by Cardiac Assist, Inc Due to A software update (v1.1.5)...
The Issue: A software update (v1.1.5) has been developed to address the issue of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Invisalign Express 10 Invisalign System Comprehensive Recalled by Align...
The Issue: 3D orthodontic planning software has a defect that leads to an issue where...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oncentra Brachy radiation therapy planning system software. Recalled by...
The Issue: A reconstruction error may occur when using the Catheter Bending...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Turbett Surgical Container Recalled by Turbett Surgical, Inc. Due to Pod may...
The Issue: Pod may have weld failures breaching the sterile barrier and result in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Remington MEDICAL Recalled by Remington Medical, Inc. Due to The stylet is...
The Issue: The stylet is longer than specified on the label
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monosof Monofilament Nylon sutures: Product Description CN-724 MONOSOF* 1...
The Issue: Sterile Barrier Breach of Breather Pouch may cause infection or vision loss...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Codman Surgical Patties Recalled by Integra LifeSciences Corp. Due to...
The Issue: Integra LifeSciences identified that one lot was released with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Surgidac Uncoated Braided Polyester suture Product Description D-1764K...
The Issue: Sterile Barrier Breach of Breather Pouch may cause infection or vision loss...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Novafil Monofilament Polybutester Suture Product Description: 8886 4002-41...
The Issue: Sterile Barrier Breach of Breather Pouch may cause infection or vision loss...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monofilament Nylon Suture (McKesson Branded) and Coated Braided Silk Suture...
The Issue: Sterile Barrier Breach of Breather Pouch may cause infection or vision loss...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.