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. 2,278 recalls have been distributed to New Hampshire in the last 12 months.
Showing 44321–44340 of 49,311 recalls
Recalled Item: QUADROX iD HMOD 2030 Diffusion Membrane Oxygenator Recalled by Maquet...
The Issue: The manufacturer has conducted a review of the results of product testing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DMLC IV-ERGO - Beam shaping block for Radiation Therapy. Recalled by Elekta,...
The Issue: Clinical mistreatment may occur when there are errors in the clinical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Propofol Injectable Emulsion Recalled by Hospira Inc. Due to Presence of...
The Issue: Presence of Particulate Matter: Visible particulate embedded in the glass...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lidocaine Hydrochloride 2% and Epinephrine 1:100 Recalled by Novocol...
The Issue: Subpotent Drug; Two lots of Lidocaine 2% with Epinephrine 1:100,000...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HEART CATH CUSTOM PACK Recalled by Medline Industries, Inc. Due to Guidewire...
The Issue: Guidewire .035x150 3MMJ TCFC, item number 88241, has a potential for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CATH TRAY Recalled by Medline Industries, Inc. Due to Guidewire .035x150...
The Issue: Guidewire .035x150 3MMJ TCFC, item number 88241, has a potential for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CATH PACK Recalled by Medline Industries, Inc. Due to Guidewire .035x150...
The Issue: Guidewire .035x150 3MMJ TCFC, item number 88241, has a potential for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STERILE SAMPLE BUILD Recalled by Medline Industries, Inc. Due to Guidewire...
The Issue: Guidewire .035x150 3MMJ TCFC, item number 88241, has a potential for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STERILE SAMPLE BUILD Recalled by Medline Industries, Inc. Due to Guidewire...
The Issue: Guidewire .035x150 3MMJ TCFC, item number 88241, has a potential for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CATH PACK Recalled by Medline Industries, Inc. Due to Guidewire .035x150...
The Issue: Guidewire .035x150 3MMJ TCFC, item number 88241, has a potential for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STERILE SAMPLE CATH LAB PACK Recalled by Medline Industries, Inc. Due to...
The Issue: Guidewire .035x150 3MMJ TCFC, item number 88241, has a potential for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CATH ANGIOGRAPHY DRAPE PACK Recalled by Medline Industries, Inc. Due to...
The Issue: Guidewire .035x150 3MMJ TCFC, item number 88241, has a potential for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ANGIO PACK #2 Recalled by Medline Industries, Inc. Due to Guidewire .035x150...
The Issue: Guidewire .035x150 3MMJ TCFC, item number 88241, has a potential for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ANGIOGRAPHY PACK Recalled by Medline Industries, Inc. Due to Guidewire...
The Issue: Guidewire .035x150 3MMJ TCFC, item number 88241, has a potential for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CATH LAB CUSTOM PACK Recalled by Medline Industries, Inc. Due to Guidewire...
The Issue: Guidewire .035x150 3MMJ TCFC, item number 88241, has a potential for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Draeger Fabius GS Premium Recalled by Draeger Medical, Inc. Due to During...
The Issue: During final testing of the Draeger Fabius GS Premium, Fabius OS, and Fabius...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CARBOplatin Injection Recalled by Teva Pharmaceuticals USA, Inc. Due to Lack...
The Issue: Lack of Assurance of Sterility: The required reduction of endotoxin was not...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Siemens EasyLink Informatics System V4.0/V5 Siemens Recalled by Siemens...
The Issue: May not perform as intended under certain conditions, causing the release of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Application Instrument Sternal Zip Flex System intended for use...
The Issue: When using the 1st generation Zip Fix Application Instrument it is possible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MedStream Programmable Pump Recalled by Codman & Shurtleff, Inc. Due to Drug...
The Issue: Drug flow rates exceeding programmed flow rates.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.