Archive
534 recalls were announced in January 2020.
Of the 534 recalls this month scored against our rubric, 7% are Critical, 40% are Severe.
Which agencies issued them
Gourmet International Ltd. is recalling Butler's Dark Chocolate with Irish Whisky bars due to undeclared milk. The recall affects 2,000 units distributed across 15 states.
Emesa Foods is recalling Premium Sesame Tahini because the product tested positive for Salmonella. The recall affects 23 cases distributed in Michigan and Texas.
Middlefield Original Cheese Coop is recalling 80 lbs of shredded Parmesan cheese due to potential Listeria monocytogenes contamination. The product was distributed to a single consignee in Ohio.
Middlefield Original Cheese Coop is recalling shredded mozzarella cheese due to potential Listeria monocytogenes contamination. The product was distributed to a single consignee in Ohio.
Motto International Corp is recalling Bull Platinum 30000 Capsules because FDA analysis found the product contains tadalafil, a prescription drug, and it was marketed without an approved NDA or ANDA.
Dierbergs Markets is recalling Deviled Egg Salad because the hardboiled eggs used were potentially contaminated with Listeria monocytogenes.
Dierbergs Markets is recalling 12-ounce containers of Kitchen Remoulade because the product was made with hardboiled eggs potentially contaminated with Listeria monocytogenes.
Middlefield Original Cheese Coop is recalling shredded cheddar cheese due to potential Listeria monocytogenes contamination. The product was distributed to a single consignee in Ohio.
Hikma Pharmaceuticals is recalling specific lots of Ketorolac Tromethamine Injection because of the presence of polydimethylsiloxane particles.
Motto International Corp is recalling Panther Platinum 30000 Capsules because FDA analysis found the product contains tadalfil and was marketed without an approved NDA or ANDA.
Motto International Corp is recalling Rhino 7 Platinum 30000 Capsules because FDA analysis found the product contains tadalafil, an unapproved active ingredient.
Fresh Unlimited Inc is recalling Chef Salad Kits because eggs used in manufacturing may be contaminated with Listeria monocytogenes.
Dierbergs Markets is recalling Creamy Red Potato Salad because it was made with hardboiled eggs potentially contaminated with Listeria monocytogenes.
Dierbergs Markets is recalling 456 salad kits because they contain hardboiled eggs potentially contaminated with Listeria monocytogenes.
Fresh Unlimited Inc is recalling Garden Salad Kits because eggs used in their manufacture may be contaminated with Listeria monocytogenes.
Assurance Infusion is recalling 190 vials of Quadmix injection nationwide due to a lack of sterility assurance. The recall covers nine specific lots distributed across the United States.
Assurance Infusion is recalling specific lots of Sufentanil 300mcg/mL injection syringes due to a lack of sterility assurance.
Assurance Infusion is recalling BUP 1MG//ML/HYDROM 7MG Injection in 20 mL syringes due to a lack of sterility assurance. The recall covers nationwide distribution in the United States.
Assurance Infusion is recalling Hydrom and Prialt injection syringes due to a lack of sterility assurance. The product was distributed nationwide in the United States.
Assurance Infusion is recalling specific lots of HCG 10,000U/1ML injections due to a lack of sterility assurance. The affected products were distributed nationwide.
Assurance Infusion is recalling specific lots of Hydromorphone 6mg/mL injection due to a lack of sterility assurance.
Assurance Infusion is recalling BUP 3MG/HYDROM 15MG/ML INJ syringes due to a lack of sterility assurance. The recall covers nationwide distribution.
Assurance Infusion is recalling specific lots of Buprenorphine and Morphine injection due to a lack of sterility assurance.
Assurance Infusion is recalling specific syringes of Baclofen, Fentanyl, and Morphine injection due to a lack of sterility assurance.
Assurance Infusion is recalling a specific lot of BUP 20MG/CLON 300MCG/FENT 2000MCG/ML Injection due to a lack of sterility assurance.
Assurance Infusion is recalling Buprenorphine and Hydromorphone Injection in 20 mL syringes due to a lack of sterility assurance. The product was distributed nationwide.
Assurance Infusion is recalling LIPO B 25MG/50MG/50MG/1000MCG/ML products due to a lack of sterility assurance. The recall covers nationwide distribution.
Assurance Infusion is recalling BUP 17MG/MORP 22MG/ML injection syringes due to a lack of sterility assurance.
Assurance Infusion is recalling a specific lot of Clonidine and Morphine injection due to a lack of sterility assurance. The product was distributed nationwide.
Assurance Infusion is recalling Hydromorphone 4mg/mL injection syringes due to a lack of sterility assurance. The product was distributed nationwide.
Assurance Infusion is recalling 20 vials of Trimix Forte Plus injection due to a lack of sterility assurance. The product was distributed nationwide.
Assurance Infusion is recalling specific lots of Morphine 1mg/mL injection syringes due to a lack of sterility assurance. The affected products were distributed nationwide.
Assurance Infusion is recalling BUP 5MG/MORP 10MG/ML Injection in 20 mL syringes due to a lack of sterility assurance. The recall covers lots distributed nationwide.
Assurance Infusion is recalling specific lots of Baclofen and Hydromorphone injection due to a lack of sterility assurance.
Assurance Infusion is recalling Fentanyl 1000mcg/mL injection syringes nationwide due to a lack of sterility assurance.
Assurance Infusion is recalling specific lots of Morphine 20mg/mL injection syringes nationwide due to a lack of sterility assurance.
Assurance Infusion is recalling specific lots of Buprenorphine and Morphine injection due to a lack of sterility assurance. The affected product was distributed nationwide.
Assurance Infusion is recalling specific lots of Morphine 18mg/mL injection due to a lack of sterility assurance. The product was distributed nationwide.
Assurance Infusion is recalling QUADMIX in 1 mL vials because of a lack of sterility assurance. The affected lot was distributed nationwide.
Assurance Infusion is recalling Hydromorphone 1mg/mL injection syringes due to a lack of sterility assurance. The product was distributed nationwide in the United States.
Assurance Infusion is recalling specific lots of Testosterone Cypionate 200mg/mL oil due to a lack of sterility assurance. The affected vials were distributed nationwide.
Assurance Infusion is recalling specific lots of Buprenorphine and Fentanyl injection due to a lack of sterility assurance.
Assurance Infusion is recalling specific lots of Buprenorphine and Hydromorphone injection due to a lack of sterility assurance.
Assurance Infusion is recalling Morphine 15mg/mL injection syringes due to a lack of sterility assurance. The recall covers products distributed nationwide in the United States.
Assurance Infusion is recalling specific lots of a Clonazepam and Morphine injection because of a lack of sterility assurance. The product was distributed nationwide.
Toyota is recalling 1997-2000 Celica, RAV4, and Supra vehicles because driver air bag inflators may rupture or underinflate in a crash.
Assurance Infusion is recalling specific lots of multi-drug injection syringes because of a lack of sterility assurance.
Assurance Infusion is recalling a specific lot of buprenorphine and fentanyl injection due to a lack of sterility assurance. The product was distributed nationwide.
Assurance Infusion is recalling specific lots of Morphine 6mg/mL injection syringes due to a lack of sterility assurance. The products were distributed nationwide.
Assurance Infusion is recalling specific lots of a multi-drug injection syringe due to a lack of sterility assurance.
Assurance Infusion is recalling QUADMIX FORTE in 1 mL vials because of a lack of sterility assurance. The recall covers 5 vials distributed nationwide.
Assurance Infusion is recalling Fentanyl 800mcg/mL injection syringes due to a lack of sterility assurance. The product was distributed nationwide in the United States.
Assurance Infusion is recalling specific lots of Hydromorphone 3mg/mL injection syringes due to a lack of sterility assurance. The products were distributed nationwide.
Assurance Infusion is recalling specific lots of Morphine 10mg/mL injection syringes nationwide due to a lack of sterility assurance.
Assurance Infusion is recalling Morphine Sulfate Injection in 20 mL syringes due to a lack of sterility assurance. The product was distributed nationwide.
Assurance Infusion is recalling specific lots of Morphine 5mg/mL injection syringes due to a lack of sterility assurance.
Assurance Infusion is recalling specific syringes of a multi-drug injection due to a lack of sterility assurance. The product was distributed nationwide.
Assurance Infusion is recalling BUP 35MG/MORP 10MG/ML Injection syringes due to a lack of sterility assurance. The product was distributed nationwide.
Edwards Lifesciences is recalling QuickDraw Venous Cannulas because the device may separate from its connector if used for more than six hours, potentially causing significant blood loss.
Assurance Infusion is recalling 45 vials of Trimix Super injection nationwide due to a lack of sterility assurance.
Assurance Infusion is recalling BUP 4MG/FENT 3000MCG/ML Injection in 20 mL syringes due to a lack of sterility assurance.
Assurance Infusion is recalling specific lots of Buprenorphine and Fentanyl injection due to a lack of sterility assurance.
Assurance Infusion is recalling Fentanyl 3000mcg/mL injection syringes due to a lack of sterility assurance. The affected lots were distributed nationwide.
Assurance Infusion is recalling specific lots of HCG 3000U/1ML injections because they lack sterility assurance. The recall covers products distributed nationwide.
Assurance Infusion is recalling Fentanyl 100mcg/mL injection syringes nationwide due to a lack of sterility assurance.
Assurance Infusion is recalling specific lots of Baclofen and Hydromorphone injection due to a lack of sterility assurance. The affected product was distributed nationwide.
Assurance Infusion is recalling Hydromorphone 20mg/mL injection syringes due to a lack of sterility assurance. The product was distributed nationwide.
Assurance Infusion is recalling specific lots of Morphine 7mg/mL injection syringes due to a lack of sterility assurance. The product was distributed nationwide.
Assurance Infusion is recalling BPC-157 vials nationwide because the product lacks sterility assurance.
Assurance Infusion is recalling Fentanyl and Sufentanil Injection due to a lack of sterility assurance. The product was distributed nationwide.
Assurance Infusion is recalling 166 vials of Testosterone Cypionate 200mg/mL oil injection due to a lack of sterility assurance. The product was distributed nationwide.
Assurance Infusion is recalling 358 vials of Trimix Forte injection nationwide due to a lack of sterility assurance.
Sun Pharmaceutical Industries is recalling Testosterone Cypionate for Injection due to cGMP deviations and similarity to a previously rejected out-of-specification lot.
Assurance Infusion is recalling 19 vials of CJC-1295 and Ipamorelin injections nationwide due to a lack of sterility assurance.
Assurance Infusion is recalling specific lots of Baclofen and Fentanyl Injection due to a lack of sterility assurance. The product was distributed nationwide.
AvKARE Inc. is recalling specific lots of Dutasteride Capsules, 0.5 mg, because they failed impurity and degradation specifications.
Assurance Infusion is recalling Fentanyl 2000mcg/mL injection syringes because of a lack of sterility assurance. The recall covers products distributed nationwide.
Hikma Pharmaceuticals is recalling specific lots of Ketorolac Tromethamine Injection because of the presence of polydimethylsiloxane particles.
Assurance Infusion is recalling Bi-Mix 30 mg/1 mg/mL injections because of a lack of sterility assurance. The affected vials were distributed nationwide.
Assurance Infusion is recalling BUP 2MG/HYDROM 2MG/ML Injection syringes due to a lack of sterility assurance. The recall covers nationwide distribution.
Assurance Infusion is recalling 20 mL syringes of BUP 15MG/CLON 600MCG/MORP 30MG/ML injection due to a lack of sterility assurance.
Assurance Infusion is recalling specific syringes containing a combination of drugs due to a lack of sterility assurance.
Assurance Infusion is recalling a specific lot of multi-drug injection syringes due to a lack of sterility assurance. The product was distributed nationwide.
Assurance Infusion is recalling Alprostadil 40 mcg/mL injection vials nationwide due to a lack of sterility assurance.
Fresh Unlimited Inc is recalling 8lb Cobb Salad Kits because eggs used in production may be contaminated with Listeria monocytogenes.
Assurance Infusion is recalling specific lots of a multi-drug injection syringe due to a lack of sterility assurance.
Assurance Infusion is recalling specific lots of Morphine 2mg/mL injection syringes due to a lack of sterility assurance.
Assurance Infusion is recalling two syringes of Phenol 2.5% Sterile Solution because of a lack of sterility assurance.
Assurance Infusion is recalling Hydrom 10mg/Suf 200mcg/mL injection syringes due to a lack of sterility assurance. The recall covers nationwide distribution.
Assurance Infusion is recalling Bi-Mix Forte 30 mg/2 mg/mL injections because of a lack of sterility assurance. The affected lot was distributed nationwide.
Assurance Infusion is recalling 10 vials of Trimix-A injection due to a lack of sterility assurance. The product was distributed nationwide in the United States.
Assurance Infusion is recalling 134 vials of Quadmix Forte injection nationwide because the product lacks sterility assurance.
Assurance Infusion is recalling specific lots of BUP 40MG/FENT 1200MCG/SUF 400MCG/ML INJ in 20 mL syringes due to a lack of sterility assurance.
Assurance Infusion is recalling Fentanyl and Sufentanil Injection in 20 mL syringes due to a lack of sterility assurance.
Assurance Infusion is recalling specific lots of Hydromorphone 2mg/mL injection syringes because of a lack of sterility assurance.
Assurance Infusion is recalling specific lots of Ipamorelin 2000mcg/mL injections because they may lack sterility assurance.
Assurance Infusion is recalling BUP 15MG/CLON 400MCG/ FENT 6000MCG/ML INJ in 20 mL syringes due to a lack of sterility assurance.
Assurance Infusion is recalling specific lots of Trimix Forte 4 injection because the product may lack sterility assurance.
Assurance Infusion is recalling specific lots of Clonidine and Hydromorphone injection due to a lack of sterility assurance.
Assurance Infusion is recalling Hydrom 1mg/Morp 20mg/Suf 100mcg/mL injection syringes due to a lack of sterility assurance.
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