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 2568125700 of 56,506 recalls

Medical DeviceJanuary 4, 2019· Cook Inc.

Recalled Item: Bentson PTFE Wire Guide Recalled by Cook Inc. Due to The wire guide may be...

The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2019· Cook Inc.

Recalled Item: Angled Tip Ureteral Catheter Set Recalled by Cook Inc. Due to The wire guide...

The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2019· Cook Inc.

Recalled Item: Heavy Duty PTFE Wire Guide Recalled by Cook Inc. Due to The wire guide may...

The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2019· Cook Inc.

Recalled Item: Percutaneous Malecot Nephrostomy Set Recalled by Cook Inc. Due to The wire...

The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2019· Cook Inc.

Recalled Item: Percutaneous Pigtail Nephrostomy Set Recalled by Cook Inc. Due to The wire...

The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2019· Cook Inc.

Recalled Item: Universa Soft Ureteral Stent Recalled by Cook Inc. Due to The wire guide may...

The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2019· Cook Inc.

Recalled Item: Sof-Flex Multi-Lenqth Ureteral Stent Set Recalled by Cook Inc. Due to The...

The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2019· Cook Inc.

Recalled Item: Fixed Core Straight Safety Wire Guide Recalled by Cook Inc. Due to The wire...

The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2019· King Systems Corp. dba Ambu, Inc.

Recalled Item: King LTS-D Kit Size 1 Recalled by King Systems Corp. dba Ambu, Inc. Due to...

The Issue: Size 0 products were incorrectly packaged and labeled as a size 1 products.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2019· Wilson-Cook Medical Inc.

Recalled Item: Acusnare Polypectomy (Duck Bill Shaped) Snare Used with an electrosurgical...

The Issue: Complaints of the snare loop not completely retracting and/or misshaping of...

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

Class II — Potential Health HazardOngoing
DrugJanuary 3, 2019· Sun Pharmaceutical Industries, Inc.

Recalled Item: Vecuronium Bromide for Injection 20 mg* *1mg/mL when reconstituted to...

The Issue: Presence of Particulate Matter: Foreign matter identified as glass detected...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 3, 2019· Sun Pharmaceutical Industries, Inc.

Recalled Item: Vecuronium Bromide for Injection 10 mg* Recalled by Sun Pharmaceutical...

The Issue: Presence of Particulate Matter: Foreign matter identified as glass detected...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 3, 2019· Arbre Farms, Inc.

Recalled Item: Organic Green Beans Recalled by Arbre Farms, Inc. Due to Potential Listeria...

The Issue: Listeria monocytogenes

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

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 3, 2019· Century Snacks LLC

Recalled Item: Snak Club Tajin Chili & Lime Peanuts Mild 5 oz. Recalled by Century Snacks...

The Issue: Undeclared allergen; tree nuts.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 3, 2019· ICU Medical, Inc.

Recalled Item: icumedical ChemoLock Vial Spike Recalled by ICU Medical, Inc. Due to There...

The Issue: There is a potential for one lot of ChemoLock Vial Spike to contain burr...

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

Class I — Serious Health HazardOngoing
DrugJanuary 2, 2019· Baxter Healthcare Corporation

Recalled Item: Dianeal Low Calcium (2.5 mEq/L) Peritoneal Dialysis Solution with 1.5%...

The Issue: Lack of Assurance of Sterility: Confirmed customer complaints for leaks on...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 2, 2019· Lupin Pharmaceuticals Inc.

Recalled Item: Cefdinir for Oral Suspension USP Recalled by Lupin Pharmaceuticals Inc. Due...

The Issue: CGMP Deviations: Product complaints received indicating reconstituted...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 2, 2019· Heritage Pharmaceuticals, Inc.

Recalled Item: Cidofovir Injection 375mg/5mL (75mg/mL) vial injection. 5 mL vials Recalled...

The Issue: Lack of Assurance of Sterility: complaints received about dried powder on...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 2, 2019· Lupin Pharmaceuticals Inc.

Recalled Item: Cefdinir for Oral Suspension USP Recalled by Lupin Pharmaceuticals Inc. Due...

The Issue: CGMP Deviations: Product complaints received indicating reconstituted...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 2, 2019· Abbott Laboratories, Inc

Recalled Item: ARCHITECT MAGNESIUM Recalled by Abbott Laboratories, Inc Due to Abbott...

The Issue: Abbott internal testing has identified that the Magnesium urine application...

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

Class II — Potential Health HazardOngoing