Product Recalls in California
Product recalls affecting California — including food, drugs, consumer products, medical devices, and vehicles distributed to California. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,217 recalls have been distributed to California in the last 12 months.
Showing 2521–2540 of 30,923 recalls
Recalled Item: AXIOS Stent and Electrocautery- Enhanced Delivery System 8mmx8mm UPN:...
The Issue: Reported Outer sheath distal black tip detaching from the device can remain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AXIOS Stent and Electrocautery- Enhanced Delivery System 10mmx10mm UPN:...
The Issue: Reported Outer sheath distal black tip detaching from the device can remain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AXIOS Stent and Electrocautery- Enhanced Delivery System 6mmx8mm UPN:...
The Issue: Reported Outer sheath distal black tip detaching from the device can remain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AXIOS Stent and Electrocautery- Enhanced Delivery System 15mmx10mm UPN:...
The Issue: Reported Outer sheath distal black tip detaching from the device can remain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Max Mobility/Permobil Smart Drive MX2+ SpeedControl Dial use Recalled by Max...
The Issue: Due to faulty circuit board in speed control remote use in conjunction with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HOT AXIOS Stent and Electrocautery- Enhanced Delivery System 15mmx10mm UPN:...
The Issue: Reported Outer sheath distal black tip detaching from the device can remain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HOT AXIOS Stent and Electrocautery- Enhanced Delivery System 20mmx10mm UPN:...
The Issue: Reported Outer sheath distal black tip detaching from the device can remain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HOT AXIOS Stent and Electrocautery- Enhanced Delivery System 10mmx10mm UPN:...
The Issue: Reported Outer sheath distal black tip detaching from the device can remain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Max Mobility/Permobil Smart Drive MX2+ SpeedControl Dial use Recalled by Max...
The Issue: Due to faulty circuit board in speed control remote use in conjunction with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AXIOS Stent and Delivery System 10mmx10mm UPN: M00553740 Recalled by Boston...
The Issue: Reported Outer sheath distal black tip detaching from the device can remain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PERMA-HAND Silk Suture Recalled by Ethicon, LLC Due to Sutures may have an...
The Issue: Sutures may have an open seal on the primary packaging, due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PROLENE Polypropylene Suture Recalled by Ethicon, LLC Due to Sutures may...
The Issue: Sutures may have an open seal on the primary packaging, due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ETHIBOND EXCEL Polyester Suture Recalled by Ethicon, LLC Due to Sutures may...
The Issue: Sutures may have an open seal on the primary packaging, due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KARL STORZ - ENDOSKOPE Recalled by Karl Storz Endoscopy Due to Scope IFUs...
The Issue: Scope IFUs contain a reprocessing modalities that have not been reviewed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KARL STORZ - ENDOSKOPE Recalled by Karl Storz Endoscopy Due to Scope IFUs...
The Issue: Scope IFUs contain a reprocessing modalities that have not been reviewed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KARL STORZ - ENDOSKOPE Recalled by Karl Storz Endoscopy Due to Scope IFUs...
The Issue: Scope IFUs contain a reprocessing modalities that have not been reviewed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Karl Storz - Endoskope - - Optical Biopsy and Grasping Forceps Recalled by...
The Issue: Due to failure of manual cleaning validation, biopsy and grasping forceps...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KARL STORZ - ENDOSKOPE Recalled by Karl Storz Endoscopy Due to Scope IFUs...
The Issue: Scope IFUs contain a reprocessing modalities that have not been reviewed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KARL STORZ - ENDOSKOPE Recalled by Karl Storz Endoscopy Due to Scope IFUs...
The Issue: Scope IFUs contain a reprocessing modalities that have not been reviewed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra Miltex CryoSolutions Cartridges 10 Pack (23.5g N2O each) Recalled by...
The Issue: During the assembly of the cartridge to its connecting body part, the valve...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.