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. 2,839 recalls have been distributed to California in the last 12 months.

56,506 total recalls
2,839 in last 12 months

Showing 2516125180 of 56,506 recalls

Medical DeviceMarch 21, 2019· Community Products, LLC

Recalled Item: Rifton TRAM Low Base Recalled by Community Products, LLC Due to A design...

The Issue: A design change to the load-bearing quick release buckle renders the springs...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 21, 2019· Flowonix Medical Inc

Recalled Item: Prometra Programmable Pump Recalled by Flowonix Medical Inc Due to The pump...

The Issue: The pump shuts down unexpectedly if Error 115, an alarm associated with a...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 21, 2019· Conmed Corporation

Recalled Item: ConMed Anchor Tissue Retrieval System 15 MM Recalled by Conmed Corporation...

The Issue: Voids in the seal or a partial seal results in an open channel and may...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 21, 2019· Conmed Corporation

Recalled Item: ConMed Anchor Tissue Retrieval System" Recalled by Conmed Corporation Due to...

The Issue: Voids in the seal or a partial seal results in an open channel and may...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 21, 2019· Community Products, LLC

Recalled Item: Rifton E-Pacer Recalled by Community Products, LLC Due to A design change to...

The Issue: A design change to the load-bearing quick release buckle renders the springs...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 21, 2019· Conmed Corporation

Recalled Item: ConMed Anchor Tissue Retrieval System Recalled by Conmed Corporation Due to...

The Issue: Voids in the seal or a partial seal results in an open channel and may...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 21, 2019· Community Products, LLC

Recalled Item: Rifton TRAM Standard Base Recalled by Community Products, LLC Due to A...

The Issue: A design change to the load-bearing quick release buckle renders the springs...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 21, 2019· Conmed Corporation

Recalled Item: ConMed Anchor Tissue Retrieval System Recalled by Conmed Corporation Due to...

The Issue: Voids in the seal or a partial seal results in an open channel and may...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 21, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: syngo.via syngo.CT Cardiac Function Recalled by Siemens Medical Solutions...

The Issue: There is a potential risk of a wrong measurement in the annulus plane during...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 21, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: syngo.via syngo.CT Cardiac Planning Recalled by Siemens Medical Solutions...

The Issue: There is a potential risk of a wrong measurement in the annulus plane during...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 21, 2019· Flowonix Medical Inc

Recalled Item: Prometra II Programmable Pump (Clinical) Recalled by Flowonix Medical Inc...

The Issue: The pump shuts down unexpectedly if Error 115, an alarm associated with a...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 21, 2019· Conmed Corporation

Recalled Item: ConMed Anchor Tissue Retrieval System 10 MM Recalled by Conmed Corporation...

The Issue: Voids in the seal or a partial seal results in an open channel and may...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 21, 2019· Flowonix Medical Inc

Recalled Item: Prometra II Programmable Pump Recalled by Flowonix Medical Inc Due to The...

The Issue: The pump shuts down unexpectedly if Error 115, an alarm associated with a...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 21, 2019· Flowonix Medical Inc

Recalled Item: Prometra Programmer (Grand Prime) Software version 2.00.29 Recalled by...

The Issue: The pump shuts down unexpectedly if Error 115, an alarm associated with a...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 21, 2019· Flowonix Medical Inc

Recalled Item: Prometra Clinician Programmer (Touchscreen) Software version 2.00.29...

The Issue: The pump shuts down unexpectedly if Error 115, an alarm associated with a...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 21, 2019· Edwards Lifesciences, LLC

Recalled Item: EV1000 Clinical Platform Recalled by Edwards Lifesciences, LLC Due to...

The Issue: Potential for an electrical short circuit leading to possible fire hazard...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
FoodMarch 21, 2019· Impossible Foods

Recalled Item: Impossible Foods Bulk Recalled by Impossible Foods Due to Piece of plastic...

The Issue: Piece of plastic was found in bulk product.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodMarch 21, 2019· Better Made Snack Foods Inc.

Recalled Item: Better Made Snack Foods Family Size $3.99 Original Potato Chips Recalled by...

The Issue: Undeclared milk

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 20, 2019· GETINGE US SALES LLC

Recalled Item: Maquet Servo-I Ventilator System -EDI CATHETER PHT Free 6Fr/49cm 5/pkg...

The Issue: Edi Catheter labeled with wrong expiry date on single pack EDI catheter boxes

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing
Medical DeviceMarch 20, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens Digital Linear Accelerators of type: ARTISTE MV System MEVATRON...

The Issue: Advisory issued not to disable or bypass the AMP function. Disabling or...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing