Hazard Type

Other Recalls

21,986 product recalls involving other. Search official CPSC, FDA, and USDA datasets for every recall issued due to this hazard.

21,986Total Recalls
1,733Critical
7708.6MUnits Affected
All Recalls

Every Other Recall

Sorted by most recent. Click any recall for full details and safety information.

21,986 recalls
High RiskFDA
Newly Weds Foods Inc
Commercial Breader Batter; A88774 BATTER MIX X2; 30 pound case
Bakery & Grains·12,540 affected·Mar 22, 2019
High RiskFDA
Newly Weds Foods Inc
Commercial Breader Batter; A80201 BATTER MX X1; 50 pound bag
Bakery & Grains·7,750 affected·Mar 22, 2019
High RiskFDA
Newly Weds Foods Inc
Commercial Breader Batter; A85608 BATTER MX X3; 50 pound bag
Bakery & Grains·2,750 affected·Mar 22, 2019
High RiskFDA
Newly Weds Foods Inc
Commercial Breader Batter; B28989 BATTER MIX X1; 50 pound bag
Bakery & Grains·20,000 affected·Mar 22, 2019
High RiskFDA
Newly Weds Foods Inc
Commercial Breader Batter; A96289 BREADER X1; 50 pound bag
Bakery & Grains·32,900 affected·Mar 22, 2019
High RiskFDA
Newly Weds Foods Inc
Commercial Breader Batter; A99751 BREADER X1; 50 pound bag
Bakery & Grains·7,550 affected·Mar 22, 2019
High RiskFDA
Newly Weds Foods Inc
Commercial Breader Batter; A93824 BREADER X3; 50 pound bag
Bakery & Grains·12,000 affected·Mar 22, 2019
High RiskFDA
Newly Weds Foods Inc
Commercial Breader Batter; A88137 BATTER MIX X1; 50 pound bag
Bakery & Grains·2,700 affected·Mar 22, 2019
High RiskFDA
Newly Weds Foods Inc
Commercial Breader Batter; B86044 BATTER MX X1; 50 pound bag
Bakery & Grains·7,800 affected·Mar 22, 2019
High RiskFDA
Newly Weds Foods Inc
Commercial Breader Batter; B95310 BREADER X4; 35 pound bag
Bakery & Grains·12,600 affected·Mar 22, 2019
High RiskFDA
Newly Weds Foods Inc
Commercial Breader Batter; A84759 BATTER MX X1; 50 pound bag
Bakery & Grains·5,000 affected·Mar 22, 2019
RecallFDA
Auro Pharmacies Inc. Dba Central Drugs
Biotin 10 mg/mL Injection, 30 mL vial, Rx only, 511 S. Harbor Blvd., Building. F, La Habra, CA 90631, 562-352-9630.
Injectable Drugs·167 affected·Mar 22, 2019
High RiskFDA
Cardinal Health 200, Llc
ChemoPlus Chemo Spill Kit Product Code:CT4004 Product Usage: ChemoPlus chemotherapy spill kits are for the clean-up and containment...
Medical Devices·11,588 affected·Mar 22, 2019
High RiskFDA
Cardinal Health 200, Llc
ChemoPlus Chemo Spill Kit, Home Health Kit Product Code:DP5108K Product Usage: ChemoPlus chemotherapy spill kits are for the clean-...
Medical Devices·5,415 affected·Mar 22, 2019
High RiskFDA
Cardinal Health 200, Llc
ChemoPlus Protective Wrap-around Goggles Product Code:DP5030G Product Usage: ChemoPlus chemotherapy spill kits are for the clean-up...
Medical Devices·3,236 affected·Mar 22, 2019
High RiskFDA
Microline Surgical, Inc.
TLS2 Thermal Ligating Shears, Catalog Number 132-131D
Medical Devices·115 affected·Mar 22, 2019
RecallUSDA
Two Brothers Pork Skins
Two Brothers Pork Skins Retira productos de piel de cerdo debido a un error de rotulación y el incumplimiento del plan HACCP en la producción
Pork·0 affected·Mar 22, 2019
High RiskFDA
Impossible Foods
Impossible Foods Bulk, 5 lb. vacuum sealed plastic-pack. Keep Frozen; This is a plant product that is looks like and is used like groun...
Meat & Poultry·1,649 affected·Mar 21, 2019
High RiskFDA
Community Products, Llc
Rifton TRAM Standard Base, SKU K310, powered lift device
Medical Devices·3,282 affected·Mar 21, 2019
High RiskFDA
Community Products, Llc
Rifton TRAM Low Base, SKU K320, powered lift device
Medical Devices·1,079 affected·Mar 21, 2019
High RiskFDA
Ge Healthcare, Llc
NM/CT 870 CZT, Model/Catalogue/Code # H3906CW Product Usage: The GE Discovery NM/CT 670 CZT system is intended for general Nuclear Me...
Cardiac Devices·16 affected·Mar 20, 2019
High RiskFDA
Ge Healthcare, Llc
NM/CT 870 DR Product Usage: The GE Discovery NM/CT 670 system is a medical tool intended for use by appropriately trained health prof...
Medical Devices·27 affected·Mar 20, 2019
High RiskFDA
Ge Healthcare, Llc
Discovery NM/CT 670 DR Product Usage: The GE Discovery NM/CT 670 system is a medical tool intended for use by appropriately trained h...
Medical Devices·11 affected·Mar 20, 2019
High RiskFDA
Ge Healthcare, Llc
Optima NM/CT 640 Product Usage: The GE Optima NM/CT 640 system is intended for General Nuclear Medicine imaging procedures for detect...
Medical Devices·35 affected·Mar 20, 2019
High RiskFDA
Ge Healthcare, Llc
NM 830 Product Usage: The Discovery NM 630 is an all-purpose dual detector nuclear imaging system intended for general nuclear medici...
Medical Devices·37 affected·Mar 20, 2019
High RiskFDA
Ge Healthcare, Llc
NM/CT 860 Product Usage: The GE NM/CT 860 system is intended for general Nuclear Medicine imaging procedures for detection of rad...
Medical Devices·6 affected·Mar 20, 2019
High RiskFDA
Ge Healthcare, Llc
NM/CT 850 Product Usage: The GE NM/CT 850 system is intended for general Nuclear Medicine imaging procedures for detection of radiois...
Medical Devices·31 affected·Mar 20, 2019
RecallFDA
Merical, Llc
Walgreens Probiotic 12.5 Billion Active Cultures, 30 capsules; Dietary Supplement. Probiotic Blend 12.5 Billion CFU's L. rhamnosus H...
Produce·323 affected·Mar 19, 2019
High RiskFDA
Lupin Somerset
Gavilyte-N, PEG-3350, Sodium chloride, Sodium Bicarbonate and Potassium Chloride for Oral Solution, Rx only, Manufactured by Novel Labora...
Oral Drugs·76,422 affected·Mar 19, 2019
High RiskFDA
Allergan Sales, Llc
Combigan (brimonidine tartrate/timolol maleate ophthalmic solution) 0.2%/0.5% 5 mL bottles, Rx only, Allergan, Inc. Irvine, CA 92612 U.S...
Ophthalmic Drugs·72 affected·Mar 19, 2019
High RiskFDA
Carestream Health, Inc.
OnSight 3D Extremity System- X-Ray, Tomography Computed System Catalog Numbers: 1743566 (w/ Attached Console) 1743574 (w/ Remote Conso...
Medical Devices·37 affected·Mar 19, 2019
RecallFDA
Aniara Diagnostica Llc
BIOPHEN UFH Control C1, REF 224101
Medical Devices·41 affected·Mar 19, 2019
RecallFDA
Aniara Diagnostica Llc
BIOPHEN LMWH Control C4, REF 224201
Medical Devices·3 affected·Mar 19, 2019
RecallFDA
Aniara Diagnostica Llc
BIOPHEN UFH Control C2, REF 223901
Medical Devices·14 affected·Mar 19, 2019
RecallFDA
Ingenus Pharmaceuticals Llc
Diclofenac Sodium Topical Solution, 1.5% w/w, 5 FL. OZ. (150 mL) bottle, Rx Only, Manufactured for: Ingenus Pharmaceuticals, LLC, Orlando...
Topical Drugs·29,435 affected·Mar 18, 2019
High RiskFDA
Ideal Implant Incorporated
IDEAL IMPLANT Structured Breast Implant, saline breast implant, in the following sizes: 210cc, 240cc, 270cc, 300cc, 335cc, 370cc, 405cc...
Medical Implants·1,704 affected·Mar 18, 2019
RecallFDA
Advanced Bionics, Llc
HiResolution Bionic Ear System HiRes 90K Advantage CI HiFocus MS Electrode REF CI-1500-04. Cochlear Implant.
Medical Implants·4 affected·Mar 18, 2019
RecallFDA
Estee Lauder Inc
Repairwear Laser Focus Line Smoothing Cream Broad Spectrum SPF 15, packaged in a light green folding carton containing a 50 mL silver jar...
Topical Drugs·14,490 affected·Mar 15, 2019
CriticalFDA
Medtronic Vascular
SHERPA NX ACTIVE GUIDING CATHETER, 6F AL1.0, .070", REF SA6AL10. for cardiovascular use
Surgical Devices·3,302 affected·Mar 15, 2019
CriticalFDA
Medtronic Vascular
SHERPA NX ACTIVE GUIDING CATHETER, 6F JL3.0 SH, .070", REF SA6JL30SH. for cardiovascular use
Surgical Devices·49 affected·Mar 15, 2019
CriticalFDA
Medtronic Vascular
SHERPA NX ACTIVE GUIDING CATHETER, 6F, 3DRC 100CM .070", REF SA63DRC. for cardiovascular use
Surgical Devices·538 affected·Mar 15, 2019
CriticalFDA
Medtronic Vascular
SHERPA NX ACTIVE GUIDING CATHETER, 6F ERAD RIGHT SHORT TIP, .070", REF SA6ERADRST. for cardiovascular use
Surgical Devices·18 affected·Mar 15, 2019
CriticalFDA
Medtronic Vascular
SHERPA NX ACTIVE GUIDING CATHETER, 6F SL4.5, .070", REF SA6SL45. for cardiovascular use
Surgical Devices·25 affected·Mar 15, 2019
CriticalFDA
Medtronic Vascular
SHERPA NX ACTIVE GUIDING CATHETER, 6F AL2.0, .070", REF SA6AL20. for cardiovascular use
Surgical Devices·1,364 affected·Mar 15, 2019
CriticalFDA
Medtronic Vascular
SHERPA NX ACTIVE GUIDING CATHETER, 6F LCB 90CM, .070", REF SA6LCBD. for cardiovascular use
Surgical Devices·3 affected·Mar 15, 2019
CriticalFDA
Medtronic Vascular
SHERPA NX ACTIVE GUIDING CATHETER, 6F 110CM AL20, REF SA6AL20A. for cardiovascular use
Surgical Devices·3 affected·Mar 15, 2019
CriticalFDA
Medtronic Vascular
SHERPA NX ACTIVE GUIDING CATHETER, 6F SL5.0, .070", REF SA6SL50. for cardiovascular use
Surgical Devices·23 affected·Mar 15, 2019
CriticalFDA
Medtronic Vascular
SHERPA NX ACTIVE GUIDING CATHETER, 6F CHAMP2.0 SH, .070", REF SA6CHAMP20SH. for cardiovascular use
Surgical Devices·9 affected·Mar 15, 2019