Product Recalls in New Hampshire
Product recalls affecting New Hampshire — including food, drugs, consumer products, medical devices, and vehicles distributed to New Hampshire. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,367 recalls have been distributed to New Hampshire in the last 12 months.
Showing 26881–26900 of 27,899 recalls
Recalled Item: NCB¿ cancellous screw Recalled by Zimmer, Inc. Due to Zimmer Inc., is...
The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CoCr Head Recalled by Zimmer, Inc. Due to Zimmer Inc., is initiating a...
The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NCB¿-PT lateral proximal 3 hole tibial plate Recalled by Zimmer, Inc. Due to...
The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fitmore" Hip Stem Recalled by Zimmer, Inc. Due to Zimmer Inc., is initiating...
The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Multipolar¿ Bipolar Cup Liner 22 mm LD. Recalled by Zimmer, Inc. Due to...
The Issue: Zimmer Inc. is initiating a removal of the Multipolar¿ Bipolar Cup Liner 22...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Wound Pro Apex Negative Pressure Wound Therapy Powered Suction Pump Recalled...
The Issue: Accuro has received reports of some Apex Pumps either failing to operate or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Brilliance CT Big Bore is a whole-body Computed Tomography Recalled by...
The Issue: Philips Healthcare received a complaint stating the system opens e-stop...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
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: 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: 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: 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: 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: 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: The Brilliance CT 16 System Product Usage: The Brilliance 16 Recalled by...
The Issue: Philips was notified that the system logout in software version 2.3.6 is now...
Recommended Action: Stop using. Contact the manufacturer or your 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: Sekisui Spectrolyse PAI-1 Recalled by Sekisui Diagnostics Llc Due to...
The Issue: SPECTROLYSE PAI-1 activity assay producing lower than expected absorbance...
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.