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. 1,089 recalls have been distributed to California in the last 12 months.
Showing 30081–30100 of 56,506 recalls
Recalled Item: ADVIA Centaur BNP (B-type Natriuretic Peptide) Recalled by Siemens...
The Issue: In certain scenarios the ADVIA Centaur CP, XP and XPT immunoassay analyzers...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spice Supreme Beef Flavored Bouillon Cubes 1.7 oz (48 g) Recalled by Gel...
The Issue: Gel Spice, Inc. is recalling three beef flavored bouillon cube products...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Spice Supreme Beef Flavored Bouillon Cubes 1.7 oz (48 g) Recalled by Gel...
The Issue: Gel Spice, Inc. is recalling three beef flavored bouillon cube products...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: ACUVUE OASYS for ASTIGMATISM Brand Contact Lenses. Lot no. B00NKM0G....
The Issue: Package integrity failure observed during routine shift package integrity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Methylphenidate Hydrochloride Extended-release Tablets Recalled by Osmotica...
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Methylphenidate Hydrochloride Extended-release Tablets Recalled by Osmotica...
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 0.25% Acetic Acid Irrigation USP Recalled by B. Braun Medical Inc Due to...
The Issue: Presence of Particulate Matter: identified as polyethylene, which is...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fosphenytoin Sodium Injection Recalled by Amneal Pharmaceuticals Due to...
The Issue: Presence of particulate matter
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Gabapentin Oral Solution Recalled by Akorn Inc Due to CGMP Deviations:...
The Issue: CGMP Deviations: Inadvertent release of a drug product with unapproved...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BrightView X Recalled by Philips Medical Systems (Cleveland) Inc Due to...
The Issue: During collimator exchange, the alignment of the collimator cart and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Uterine Electromyographic Monitor - Monica Novii Wireless Patch System...
The Issue: if the cables of the Monica Novii System are removed by a user, and then...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Precedence 16 Model # 882350 Product Usage: Precedence (cleared as Recalled...
The Issue: During collimator exchange, the alignment of the collimator cart and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Uterine Electromyographic Monitor -Monica IF24 Interface System Product...
The Issue: if the cables of the Monica IF24 System are removed by a user, and then...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BrightView XCT Model 882482 Product Usage: BrightView XCT is a Recalled by...
The Issue: During collimator exchange, the alignment of the collimator cart and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BrightView Model 882480 Product Usage: BrightView and BrightView X are...
The Issue: During collimator exchange, the alignment of the collimator cart and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Precedence 6 Model # 882351 Product Usage: Precedence (cleared as Recalled...
The Issue: During collimator exchange, the alignment of the collimator cart and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2008 K2 Hemodialysis Machine with software version 5.40 Recalled by...
The Issue: When the recirculation ultrafiltration (UF) Goal is set to a value greater...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARCHITECT DHEA-S Reagent Product Usage: It is a chemiluminescent...
The Issue: Falsely elevated results may be obtained when using the ARCHITECT DHEA-S...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Shiseido Future Solution LX Universal Defense SPF 50+ (octinoxate 4.9%...
The Issue: GMP Deviations: manufacturing of API material did not meet GMP and quality...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SPIRIVA HandiHaler (tiotropium bromide inhalation powder) 18 mcg/capsule (90...
The Issue: Failed Stability Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.