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. 2,893 recalls have been distributed to California in the last 12 months.
Showing 18021–18040 of 30,923 recalls
Recalled Item: VERSYS 8 INCH BEADED FC 12X200MM STR STD BODY/NECK 13X200MM Recalled by...
The Issue: The LDPE bag packaging for various highly polished hip and knee implants may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VERSYS 7.5 IN BEADED FC +10 CALCAR 13.5X180MM STR +10 Recalled by Zimmer...
The Issue: The LDPE bag packaging for various highly polished hip and knee implants may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BCI Advisor Vital Signs Monitor Recalled by Smiths Medical ASD Inc. Due to...
The Issue: Some printing modes on the devices may not function properly (tabular data...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: lmmunalysis EDDP Urine Control Set 1 The EDDP Urine Controls Recalled by...
The Issue: The High (125 ng/ml) Control does not meet specification - it has been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Syva¿ EMIT¿ 2000 Theophylline Product Usage: The Syva¿ Emit¿ 2000 Recalled...
The Issue: Lot J1 of the Syva¿ EMIT¿ 2000 Theophylline Assay, when run on a Beckman AU...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRYPTIK(R) 2 C-PLATE SELF-TAPPING POLYAXIAL SCREW 4.0 MM Recalled by...
The Issue: Product labeling for TRYPTIK 2-C-PLATE Self Tapping screw, 40, Lot 3-5934...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRYPTIK(R) 2 C-PLATE SELF-TAPPING POLYAXIAL SCREW 4.5 MM Recalled by...
The Issue: Product labeling for TRYPTIK 2-C-PLATE Self Tapping screw, 40, Lot 3-5934...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRYPTIK(R) 2 C-PLATE SELF-TAPPING POLYAXIAL SCREW 4.0 MM Recalled by...
The Issue: Product labeling for TRYPTIK 2-C-PLATE Self Tapping screw, 40, Lot 3-5934...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DERMABOND" PRINEO" Skin Closure System Product Usage: DERMABOND PRINEO...
The Issue: Ethicon discovered that specific lots of DERMABOND"PRINEO"System may not dry...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRYPTIK(R) 2 C-PLATE SELF-TAPPING POLYAXIAL SCREW 4.5 MM Recalled by...
The Issue: Product labeling for TRYPTIK 2-C-PLATE Self Tapping screw, 40, Lot 3-5934...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRYPTIK(R) 2 C-PLATE SELF-TAPPING POLYAXIAL SCREW 4.5 MM Recalled by...
The Issue: Product labeling for TRYPTIK 2-C-PLATE Self Tapping screw, 40, Lot 3-5934...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRYPTIK(R) 2 C-PLATE SELF-TAPPING POLYAXIAL SCREW 4.5 MM Recalled by...
The Issue: Product labeling for TRYPTIK 2-C-PLATE Self Tapping screw, 40, Lot 3-5934...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRYPTIK(R) 2 C-PLATE SELF-TAPPING POLYAXIAL SCREW 4.0 MM Recalled by...
The Issue: Product labeling for TRYPTIK 2-C-PLATE Self Tapping screw, 40, Lot 3-5934...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hemotherm¿ Dual Reservoir Cooler/Heater System Models 400CE and 400MR...
The Issue: Due to FDA's safety communication relating to nontuberculous mycobacteria...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8F Plastic Dignity¿ Low Profile CT Port W/Pre-Attached ChronoFlex¿...
The Issue: The kit was packaged with the incorrect guidewire. The label indicates the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ECOLAB MICROTEK Rolled Probe Cover Recalled by ECOLAB INC Due to The...
The Issue: The incorrect IFU was shipped with the product.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ECOLAB MICROTEK Rolled Probe Cover Recalled by ECOLAB INC Due to The...
The Issue: The incorrect IFU was shipped with the product.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Santajoy Ornament & Giftware Co. Recalled by SANTA JOY ORNAMENT & GIFTWARE...
The Issue: It was discovered that the product units it imported may, at peak levels,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OCULUS Pentacam AXL Recalled by Oculus Optikgeraete GMBH Due to The device...
The Issue: The device software versions have an anomaly which may produce an erroneous...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rechargeable Li-ion battery used with Puritan Bennett TM 980 Series Recalled...
The Issue: Rechargeable lithium-ion batteries with incorrect firmware that are used in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.