New Hampshire recalls
3272 federal recalls on file affecting New Hampshire - 195 New Hampshire-specific plus 3077 nationwide. Sourced from CPSC, FDA, USDA, and NHTSA.
- 2025-11-05FDA-DeviceMicroSurgical TechnologyClass IINationwideMST ArcDUO 9mm, REF: ARC-0002, single-use, sterile ophthalmic knife, used with Suction Set, Part: 48-1000-01
An ophthalmic knife has a suction set (not direct patient-contacting), which contains springs contaminated with an unidentified residue that may potentially cause eye irritation
- 2025-11-05FDA-DeviceVantiveClass IINationwideSharesource Connectivity Platform for Use with Homechoice Claria Product Code 5CGM01 software versions 7.13.3 (China), 8.13.2 (APAC and Korea), and 8.13.4 (US, EMEA, and LATAM)
Vantive has identified a software defect within the Sharesource Claria software, which may cause a patient s updated prescription program settings to not be properly saved on the actual cycler that the patient is using to perform their therapy. As a result, the clinician may think that the patient is receiving the correct prescribed therapy because of what is erroneously displayed on the clinician's remote Sharesource application, when in fact the cycler that is with the patient is actually delivering an outdated and incorrect therapy.
- 2025-11-05FDA-DeviceGreiner Bio-OneClass IINationwideGreiner BIO-ONE VACUETTE 2 ml 9NC Coagulation sodium citrate 3.2%, REF: 454322
Blood collection tubes were manufactured with the label applied too high on the tube, which shifted the printed fill level mark upward, which could result in unnecessary sample rejection and repeat collections.
- 2025-11-05FDA-DeviceDayeClass IINationwideInitiation 3 Month Heavy Flow Bundle; Model Number: FG-BNDL-PC-MM-IBHF;
Product lacks 510(k) clearance.
- 2025-11-05FDA-DeviceDayeClass IINationwideInitiation 3 Month Regular Flow Bundle; Model Number: FG-BNDL-PC-MM-IBRF;
Product lacks 510(k) clearance.
- 2025-11-05FDA-DeviceDayeClass IINationwideInitiation 3 Month All in One Bundle; Model Number: FG-BNDL-PC-MM-IBAIO;
Product lacks 510(k) clearance.
- 2025-11-05FDA-DeviceDayeClass IINationwideInitiation 3 Month Trial Tampon Box; Model Number: FG-TMP-MM-IB09090909;
Product lacks 510(k) clearance.
- 2025-11-05FDA-DeviceDayeClass IINationwideInitiation 18 Coated Super and 18 Nude Super Tampons; Model Number: FG-TMP-MM-IB00180018;
Product lacks 510(k) clearance.
- 2025-11-05FDA-DeviceDayeClass IINationwideInitiation 18 Coated Regular and 18 Nude Regular Tampons; Model Number: FG-TMP-MM-IB18001800;
Product lacks 510(k) clearance.
- 2025-11-05FDA-DeviceDayeClass IINationwideInitiation 18 Coated Regular and 18 Coated Super Tampons; Model Number: FG-TMP-MM-IB18180000;
Product lacks 510(k) clearance.
- 2025-11-05FDA-DeviceDayeClass IINationwideInitiation 36 Coated Super Tampons; Model Number: FG-TMP-MM-IB00360000;
Product lacks 510(k) clearance.
- 2025-11-05FDA-DeviceDayeClass IINationwideInitiation 36 Coated Regular Tampons; Model Number: FG-TMP-MM-IB36000000;
Product lacks 510(k) clearance.
- 2025-11-05FDA-DeviceDayeClass IINationwideRefill 3 Month Heavy Flow Bundle; Model Number: FG-BNDL-PC-MM-REFHF;
Product lacks 510(k) clearance.
- 2025-11-05FDA-DeviceDayeClass IINationwideRefill 3 Month Regular Flow Bundle; Model Number: FG-BNDL-PC-MM-REFRF;
Product lacks 510(k) clearance.
- 2025-11-05FDA-DeviceDayeClass IINationwideRefill 3 Month All in One Bundle; Model Number: FG-BNDL-PC-MM-REFAIO;
Product lacks 510(k) clearance.
- 2025-11-05FDA-DeviceDayeClass IINationwideRefill 3 Month Trial Tampon Box; Model Number: FG-TMP-MM-REF09090909;
Product lacks 510(k) clearance.
- 2025-11-05FDA-DeviceDayeClass IINationwideRefill 18 Coated Super and 18 Nude Super Tampons; Model Number: FG-TMP-MM-REF00180018;
Product lacks 510(k) clearance.
- 2025-11-05FDA-DeviceDayeClass IINationwideRefill 18 Coated Regular and 18 Nude Regular Tampons; Model Number: FG-TMP-MM-REF18001800;
Product lacks 510(k) clearance.
- 2025-11-05FDA-DeviceDayeClass IINationwideRefill 18 Coated Regular and 18 Coated Super Tampons; Model Number: FG-TMP-MM-REF18180000;
Product lacks 510(k) clearance.
- 2025-11-05FDA-DeviceDayeClass IINationwideRefill 36 Coated Super Tampons; Model Number: FG-TMP-MM-REF00360000;
Product lacks 510(k) clearance.
- 2025-11-05FDA-DeviceDayeClass IINationwideRefill 36 Coated Regular Tampons; Model Number: FG-TMP-MM-REF36000000;
Product lacks 510(k) clearance.
- 2025-11-05FDA-DeviceDayeClass IINationwideHeavy Flow Bundle; Model Number: FG-BNDL-PC-REFHF;
Product lacks 510(k) clearance.
- 2025-11-05FDA-DeviceDayeClass IINationwideRegular Flow Bundle; Model Number: FG-BNDL-PC-REFRF;
Product lacks 510(k) clearance.
- 2025-11-05FDA-DeviceDayeClass IINationwideAll in One Bundle; Model Number: FG-BNDL-PC-REFAIO;
Product lacks 510(k) clearance.
- 2025-11-05FDA-DeviceDayeClass IINationwideTrial Tampon Box; Model Number: FG-TMP-REF04050504;
Product lacks 510(k) clearance.
- 2025-11-05FDA-DeviceDayeClass IINationwide9 Coated Super and 9 Nude Super Tampons; Model Number: FG-TMP-REF00090009;
Product lacks 510(k) clearance.
- 2025-11-05FDA-DeviceDayeClass IINationwide9 Coated Regular and 9 Nude Regular Tampons; Model Number: FG-TMP-REF09000900;
Product lacks 510(k) clearance.
- 2025-11-05FDA-DeviceDayeClass IINationwide9 Coated Regular and 9 Coated Super Tampons; Model Number: FG-TMP-REF09090000;
Product lacks 510(k) clearance.
- 2025-11-05FDA-DeviceDayeClass IINationwide18 Coated Super Tampons; Model Number: FG-TMP-REF00180000;
Product lacks 510(k) clearance.
- 2025-11-05FDA-DeviceDayeClass IINationwide18 Coated Regular Tampons; Model Number: FG-TMP-REF18000000;
Product lacks 510(k) clearance.
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