State

New Hampshire product recalls

73,817 recalls have nationwide distribution and so reach New Hampshire. 4,483 additional recalls listed New Hampshire specifically in their distribution scope.

What the numbers show

Total: 4,483
Critical: 603
Severe: 1,049
Most recent: 2026-11-04

Of the 4,483 recalls naming New Hampshire we have scored against our rubric, 603 (13%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,049 (23%) are Severe.

Which agencies issued them

These figures cover only the 4,483 recalls whose distribution notice names New Hampshire specifically. The 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

45876–45900 of 78300

SevereFDA (Drugs)·D-0779-2017·2017-05-24
Key Pharmacy Recalls Sodium Carboxymethylcellulose Ophthalmic Solution Due to Sterility Concerns
Key Pharmacy and Compounding Center is recalling specific lots of Sodium Carboxymethylcellulose 0.5% Ophthalmic Solution because the firm cannot ensure the product is sterile.
Product
SODIUM CARBOXYM-CELL PF 0.5% OPHTH, opthalmic, 0.50%, Rx only, 10mL Glass/Multiple Dose vial, Prepared by Key Compounding Pharmacy
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0754-2017·2017-05-24
Key Pharmacy Recalls Compounded Quad Mix Injection Due to Sterility Concerns
Key Pharmacy and Compounding Center is recalling specific lots of Quad Mix injection due to a lack of assurance of sterility.
Product
QUAD MIX 1/30/0.5/0.1 5ML MDV MCG/MG/MG/MG/ML INJ, Injection, 1mcg/30mg/0.5mg/0.15mg/mL, Rx only, 5 mL Glass/Multiple Dose vial, Prepared by Key Compounding Pharmacy
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0743-2017·2017-05-24
Key Pharmacy Recalls Sterile Compounded Injection Due to Sterility Concerns
Key Pharmacy and Compounding Center is recalling TRI MIX 20/30/0.5 injection vials due to a lack of assurance of sterility.
Product
TRI MIX 20/30/0.5 5ML MDV MCG/MG/MG/ML INJ, Injection, 20mcg/30mg/0.5mg/mL, Rx only, 5 mL Glass/Multiple Dose vial, Prepared by Key Compounding Pharmacy
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0739-2017·2017-05-24
Key Pharmacy Recalls Sterile Compounded Injection Due to Sterility Concerns
Key Pharmacy and Compounding Center is recalling a specific lot of TRI MIX injection due to a lack of assurance of sterility.
Product
TRI MIX 11.8/17.6/0.59 5ML MDV MCG/MG/MG/ML INJ, Injection, 11.8mcg/17.6mg/0.59mg/mL, Rx only, 5mL Glass/Multiple Dose vial, Prepared by Key Compounding Pharmacy
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0731-2017·2017-05-24
Key Pharmacy Recalls PGE1 Injection Due to Sterility Concerns
Key Pharmacy and Compounding Center is recalling PGE1 MDV 20mcg/mL injections due to a lack of assurance of sterility. The affected products were distributed in the U.S., Australia, and Canada.
Product
PGE1 MDV 20MCG/ML INJ, Injection, 20mcg/mL, Rx only, packaged in a 5 mL, 10mL, and 15 mL Glass/Multiple Dose vials, Prepared by Key Compounding Pharmacy
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0760-2017·2017-05-24
FDA Recalls Compounded Injection Due to Lack of Sterility Assurance
Key Pharmacy and Compounding Center is recalling CHOL/IN/ME(L)/B6 10ML MDV injection due to lack of assurance of sterility.
Product
CHOL/IN/ME(L)/B6 10ML MDV 50/50/25/0.1MG/ML INJ, Injection, 50mg/50mg/25mg/0.1mg/mL, Rx only, 10mL Glass/Multiple Dose vial, Prepared by Key Compounding Pharmacy
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0716-2017·2017-05-24
FDA Recalls Key Pharmacy Compounded Ferric Gluconate Injection for Sterility Concerns
Key Pharmacy and Compounding Center is recalling a specific lot of compounded ferric gluconate injection due to a lack of assurance of sterility.
Product
FERR GLUC/PROCAINE 10ML MDV 60/10MG/ML INJ, Injection, 60mg/10mg/mL, Rx only, 10 mL glass/Multiple Dose vial, Prepared by Key Compounding Pharmacy
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0718-2017·2017-05-24
Key Pharmacy Recalls Folinic Acid Injections Due to Sterility Concerns
Key Pharmacy and Compounding Center is recalling specific lots of Folinic Acid injections because the firm cannot guarantee the products are sterile.
Product
FOLINIC ACID MDV (CALIF) 5MG/ML INJ, Injection, 5mg/mL, Rx only, packaged in 5 mL and10 mL glass/ Multiple Dose vial, Prepared by Key Compounding Pharmacy
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0775-2017·2017-05-24
FDA Recalls Compounded Progesterone Injection Due to Sterility Concerns
Key Pharmacy and Compounding Center is recalling compounded progesterone injections because the firm cannot ensure the products are sterile.
Product
PROGESTERONE SESAME OIL 10ML MDV 100MG/ML INJ, Injection, 100mg/mL, Rx only, 10mL Glass; Multiple Dose vial, Prepared by Key Compounding Pharmacy
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0786-2017·2017-05-24
Key Pharmacy Recalls Vitamin D3 Injection Due to Sterility Concerns
Key Pharmacy and Compounding Center is recalling specific lots of Vitamin D3 in Olive Oil Injection due to a lack of assurance of sterility.
Product
VITAMIN D3 IN OLIVE OIL SDV 100,000U/ML INJ, Injection, 150,000u/mL, Rx only, packaged in 2mL Glass/Single Dose vial, Prepared by Key Compounding Pharmacy
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0728-2017·2017-05-24
Key Pharmacy Recalls Hydroxo-B12 Injections Due to Sterility Concerns
Key Pharmacy and Compounding Center is recalling specific lots of Hydroxo-B12 injections because the firm cannot guarantee the products are sterile.
Product
HYDROXO-B12 5ML PBF MDV (CALIF) 10MG/ML INJ, Injection, 10mg/mL, RX only, 5mL Glass/Multiple Dose vial, Prepared by Key Compounding Pharmacy
Category
Drug
Distribution
Distributed nationwide
HighNHTSA·17V337000·2017-05-24
MCI Recalls 2011-2012 Coaches Due to Exhaust Pipe Fire Risk
Motor Coach Industries is recalling 2011-2012 MCI D4000, D4005, D4500, and D4505 coaches because an incorrectly installed exhaust bellow pipe may bend and fail, increasing the risk of fire.
Product
MCI — MCI D4000, D4500, D4505, D4005
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0738-2017·2017-05-24
Key Pharmacy Recalls Sterile Compounded Drug Injection Due to Sterility Concerns
Key Pharmacy and Compounding Center is recalling specific lots of TRI MIX 10/30/1 injection due to a lack of assurance of sterility.
Product
TRI MIX 10/30/1 5ML MDV MCG/MG/MG/ML INJ, Injection, 10mcg/30mg/1mg/mL, Rx only, 5 mL Glass/ Multiple Dose vial, Prepared by Key Compounding Pharmacy
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0781-2017·2017-05-24
Key Pharmacy Recalls SOD Phenylbutyrate Injections Due to Sterility Concerns
Key Pharmacy and Compounding Center is recalling 91 vials of SOD Phenylbutyrate injections due to a lack of assurance of sterility.
Product
SOD PHENYLBUTYRATE SDV 30ML (CALIF or NEZ-CALIF) 200MG/ML INJ, Injection, 200mg/mL, Rx only, 30 mL Glass/Single Dose vial, Prepared by Key Compounding Pharmacy
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0734-2017·2017-05-24
Key Pharmacy Recalls Compounded PGE1/PAP Injection Due to Sterility Concerns
Key Pharmacy and Compounding Center is recalling specific lots of compounded PGE1/PAP injection because the firm cannot assure the sterility of the product.
Product
PGE1/PAP 10/30 5ML MDV MCG/MG/ML INJ, Injection, 10mg/30mg/mL, Rx only, 5mL Glass/Multiple Dose vial, Prepared by Key Compounding Pharmacy
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0708-2017·2017-05-24
Key Pharmacy Recalls 5-MTHF Injections Due to Sterility Concerns
Key Pharmacy and Compounding Center is recalling 5-MTHF 10mL multiple-dose vials due to a lack of assurance of sterility. The product was distributed in the U.S., Australia, and Canada.
Product
5-MTHF 10ML MDV (CALIF) 5MG/ML INJ, Injection, 5mg/mL, Rx only, 10mLGlass/Multiple Dose vial, Prepared by Key Compounding Pharmacy
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2087-2017·2017-05-24
Aesculap ELAN 4 Diamond Burrs Recalled for Particulate Breakage
Aesculap Implant Systems LLC is recalling 608 ELAN 4 diamond burrs because particulates may break off and enter the surgical site, potentially causing foreign body reactions or tissue damage.
Product
GP161R; ELAN 4 1-RING DIAMOND BURR COARSE D2.0; GP162R; ELAN 4 1-RING DIAMOND BURR+ COARSE D2.0; GP163R; ELAN 4 1-RING DIAMOND BURR COARSE D2,3; GP164R; ELAN 4 1-RING DIAMOND BURR+ COARSE D2,3; GP165R; ELAN 4 1-RING DIAMOND BURR COARSE D3,0; GP166R; ELAN 4…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2089-2017·2017-05-24
Aesculap Hi-Line XS Diamond Burrs Recalled for Particulate Breakage Risk
Aesculap Implant Systems LLC is recalling 608 Hi-Line XS Diamond Burrs because diamond particulates may break off and fall into the surgical site, potentially causing foreign body reactions or soft tissue damage.
Product
GE426R; HI-LINE XS DIAMOND BURR X-CRS.I D4.5MM; GE426SU; HI-LINE XS DISP.DIAM.BURR X-CRS.I D4.5MM; GE526R; HI-LINE XS DIAMOND BURR X-CRS.II D4.5MM; GE526SU; HI-LINE XS DISP.DIAM.BURR X-CRS.II D4.5; GE626R; HI-LINE XS DIAMOND BURR X-CRS.III D4.5MM; GE626SU; HI-LINE…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2095-2017·2017-05-24
BioMerieux Recalls ETEST ETP32 Ertapenem Strips Due to False Results
BioMerieux SA is recalling ETEST ETP32 (Ertapenem) strips because they may produce false susceptible results, potentially leading to incorrect antibiotic treatment.
Product
ETEST ETP32 (Ertapenem) Ref. 531640, 531600, blister packaging ETEST is a quantitative technique for determining the antimicrobial susceptibility of Gram-negative and Gram-positive aerobic bacteria (Only 531640 was distributed in the United States)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0723-2017·2017-05-24
Key Pharmacy Recalls Hydroxo-B12 Inhalation Solution Due to Sterility Concerns
Key Pharmacy and Compounding Center is recalling Hydroxo-B12 inhalation solution because the firm cannot assure the sterility of the product.
Product
HYDROXO-B12 INH PF GV 5MG/ML SOLN, Inhalation Solution, 5mg/mL, Rx only, 5 mL Glass/Multiple Dose vial, Prepared by Key Compounding Pharmacy
Category
Drug
Distribution
Distributed nationwide
HighNHTSA·17V336000·2017-05-24
Forest River Recalls Cardinal Trailers Due to Incorrect Weight Rating Labels
Forest River is recalling 2016-2018 Cardinal recreational trailers because the Federal Placard overstates the Gross Axle Weight Rating, which may lead to vehicle overloading.
Product
FOREST RIVER — FOREST RIVER CARDINAL
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2088-2017·2017-05-24
Aesculap ELAN 4 Diamond Burrs Recalled for Particulate Breakage Risk
Aesculap Implant Systems LLC is recalling ELAN 4 2-Ring Diamond Burrs because diamond particulates may break off and enter the surgical site, potentially causing foreign body reactions or tissue damage.
Product
GP321R; ELAN 4 2-RING DIAMOND BURR COARSE D2.3; GP322R; ELAN 4 2-RING DIAMOND BURR COARSE D3.0; GP323R; ELAN 4 2-RING DIAMOND BURR COARSE D4.0; GP324R; ELAN 4 2-RING DIAMOND BURR COARSE D5.0; GP325R; ELAN 4 2-RING DIAMOND BURR COARSE D6.0; Product Usage: The…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2103-2017·2017-05-24
Medline 16 mm Distraction Pin Recalled Due to Sterile Seal Integrity
Medline Industries is recalling 198 packs of 16 mm Distraction Pins because the sterile packaging seal may be compromised, risking loss of sterility.
Product
16 mm Distraction Pin, Titanium, Qty: 1 per pack; STERILE; Manufactured for: Medline Industries, Inc., Mundelein, IL 60060 USA Distraction Pin is designed for Anterior Cervical Fusion Procedures. Use with vertebral body distraction instruments. It is intended as a temporary…
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·17158·2017-05-24
Leggett & Platt Recalls Office Chairs Due to Fall Hazard
Leggett & Platt is recalling about 47,900 office chairs in the U.S. because seat slider bolts can disconnect, causing the seat to detach and posing a fall hazard.
Product
Office chairs
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2106-2017·2017-05-24
Medline 14 mm Distraction Pin Recalled for Potential Sterility Loss
Medline Industries is recalling 14 mm Distraction Pins due to potential sterile packaging seal failures that could compromise device sterility.
Product
14 mm Distraction Pin, Exagg Qty: 1 per pack; STERILE; Manufactured for: Medline Industries, Inc., Mundelein, IL 60060 USA Distraction Pin is designed for Anterior Cervical Fusion Procedures. Use with vertebral body distraction instruments. It is intended as a temporary…
Category
Medical Device
Distribution
Distributed nationwide