Product Recalls in Massachusetts
Product recalls affecting Massachusetts — including food, drugs, consumer products, medical devices, and vehicles distributed to Massachusetts. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,437 recalls have been distributed to Massachusetts in the last 12 months.
Showing 50861–50880 of 52,647 recalls
Recalled Item: Trader Joe's Tropical Fruit Medley Recalled by F & S Produce Co., Inc. (Site...
The Issue: F&S Produce Co., Inc. of Rosenhayn, NJ is initiating a voluntary recall of a...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Delish Tropical Medley 10 oz.(283 g) Enjoy by: 8/28/12 and Recalled by F & S...
The Issue: F&S Produce Co., Inc. of Rosenhayn, NJ is initiating a voluntary recall of a...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Delish Pineapple Recalled by F & S Produce Co., Inc. (Site II) Due to...
The Issue: F&S Produce Co., Inc. of Rosenhayn, NJ is initiating a voluntary recall of a...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: ATLANTIS(R) Anterior Cervical Plate System FIXED ANGLE SCREW MODULE Recalled...
The Issue: Lines on the screw gauge may not placed on the caddy properly which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PREMIER(R) Anterior Cervical Plate System SCREW BLOCK Recalled by Medtronic...
The Issue: Lines on the screw gauge may not placed on the caddy properly which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ATLANTIS(R) Anterior Cervical Plate System VARIABLE ANGLE SCREW MODULE...
The Issue: Lines on the screw gauge may not placed on the caddy properly which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Guardian II Hemostasis Valve Recalled by Vascular Solutions, Inc. Due to...
The Issue: Vascular Solutions, Inc., became aware of a potential problem involving...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BiCNU (Carmustine for injection) 100 mg and Diluent Rx Only Recalled by...
The Issue: Superpotent (Single Ingredient) Drug: All BiCNU lots within expiration which...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Propofol Injectable Emulsion Recalled by Hospira Inc. Due to Presence of...
The Issue: Presence of Particulate Matter: A single visible particulate was observed...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: T-Handle Recalled by SpineFrontier, Inc. Due to During an operation the...
The Issue: During an operation the strike plate of a T-Handle loosened and separated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Symbiq One Channel Infuser Recalled by Hospira Inc. Due to The Symbiq pump...
The Issue: The Symbiq pump touchscreen may not respond to user selection, may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Symbiq Two Channel Infuser Recalled by Hospira Inc. Due to The Symbiq pump...
The Issue: The Symbiq pump touchscreen may not respond to user selection, may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Automatic Cutting Needles Recalled by Remington Medical Inc. Due to...
The Issue: Sterility of the product may be compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diazepam Injection Recalled by Hospira Inc. Due to Lack of Assurance of...
The Issue: Lack of Assurance of Sterility: Loose crimp applied to the fliptop vial.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Preservative-Free MORPHINE Sulfate Injection Recalled by Hospira Inc. Due to...
The Issue: Lack of Assurance of Sterility: Loose crimp applied to the fliptop vial
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: I-C Drops Recalled by James G. Cole, Inc. Due to Lack of Assurance of...
The Issue: Lack of Assurance of Sterility: The product is being recalled because the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Spine Frontier Inspan compressors Part Number: 11-60004. Inspan compressors...
The Issue: Inspan Compressors may break at weld causing a loss of compression
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PREVI Isola System Recalled by Biomerieux Inc Due to The instrument may not...
The Issue: The instrument may not dispense the specimen onto the pre-poured media...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TORQ Sternal Closure Device. The common name is TWISTER Recalled by Kardium...
The Issue: The TORQ Sternal Closure Device, Lot 062711, is being recalled due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Empty Evacuated Container 250 mL and 1000 mL. Empty Evacuated Recalled by...
The Issue: Embedded iron oxide glass defect which may have the potential to break off...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.